141 related articles for article (PubMed ID: 30016051)
1. General Hospital and Personal Use Devices; Reclassification of Sharps Needle Destruction Device. Final order.
Food and Drug Administration, HHS
Fed Regist; 2018 May; 83(87):19626-8. PubMed ID: 30016051
[TBL] [Abstract][Full Text] [Related]
2. Obstetrical and Gynecological Devices; Reclassification of Single-Use Female Condom, To Be Renamed Single-Use Internal Condom. Final order.
Food and Drug Administration, HHS
Fed Regist; 2018 Sep; 83(188):48711-3. PubMed ID: 30272398
[TBL] [Abstract][Full Text] [Related]
3. Cardiovascular Devices; Reclassification of External Pacemaker Pulse Generator Devices; Reclassification of Pacing System Analyzers. Final order.
Food and Drug Administration, HHS
Fed Regist; 2016 Apr; 81(74):22525-30. PubMed ID: 27101641
[TBL] [Abstract][Full Text] [Related]
4. Dental Devices; Reclassification of Electrical Salivary Stimulator System. Final order.
Food and Drug Administration, HHS
Fed Regist; 2015 Nov; 80(224):72585-6. PubMed ID: 26595942
[TBL] [Abstract][Full Text] [Related]
5. Medical devices; general hospital and personal use devices; classification of the intravascular administration set, automated air removal system. Final order.
Food and Drug Administration, HHS
Fed Regist; 2014 May; 79(95):28404-7. PubMed ID: 24839665
[TBL] [Abstract][Full Text] [Related]
6. General and plastic surgery devices: reclassification of ultraviolet lamps for tanning, henceforth to be known as sunlamp products and ultraviolet lamps intended for use in sunlamp products. Final order.
Food and Drug Administration, HHS
Fed Regist; 2014 Jun; 79(105):31205-14. PubMed ID: 24908684
[TBL] [Abstract][Full Text] [Related]
7. Obstetrical and Gynecological Devices; Reclassification of Surgical Instrumentation for Use With Urogynecologic Surgical Mesh. Final order.
Food and Drug Administration, HHS
Fed Regist; 2017 Jan; 82(4):1598-603. PubMed ID: 28071876
[TBL] [Abstract][Full Text] [Related]
8. Medical Devices; Exemptions From Premarket Notification: Class II Devices. Final order.
Food and Drug Administration, HHS
Fed Regist; 2018 Jun; 83(108):25910-5. PubMed ID: 30019871
[TBL] [Abstract][Full Text] [Related]
9. Physical medicine devices; reclassification of stair-climbing wheelchairs. Final order.
Food and Drug Administration, HHS
Fed Regist; 2014 Apr; 79(71):20779-83. PubMed ID: 24741753
[TBL] [Abstract][Full Text] [Related]
10. Gastroenterology-urology devices; reclassification of implanted blood access devices. Final rule.
Food and Drug Administration, HHS
Fed Regist; 2014 Jul; 79(143):43241-6. PubMed ID: 25118367
[TBL] [Abstract][Full Text] [Related]
11. Orthopedic Devices; Reclassification of Pedicle Screw Systems, Henceforth To Be Known as Thoracolumbosacral Pedicle Screw Systems, Including Semi-Rigid Systems. Final order.
Food and Drug Administration, HHS
Fed Regist; 2016 Dec; 81(251):96366-74. PubMed ID: 28068051
[TBL] [Abstract][Full Text] [Related]
12. Obstetrical and Gynecological Devices; Reclassification of Surgical Mesh for Transvaginal Pelvic Organ Prolapse Repair; Final order.
Food and Drug Administration, HHS
Fed Regist; 2016 Jan; 81(2):353-61. PubMed ID: 26742182
[TBL] [Abstract][Full Text] [Related]
13. Medical Devices; General Hospital and Personal Use Devices; Classification of the Ultraviolet Radiation Chamber Disinfection Device. Final order.
Food and Drug Administration, HHS
Fed Regist; 2015 Nov; 80(224):72587-9. PubMed ID: 26595943
[TBL] [Abstract][Full Text] [Related]
14. Dental devices; reclassification of temporary mandibular condyle prosthesis. Final order.
Food and Drug Administration, HHS
Fed Regist; 2013 Dec; 78(250):79308-10. PubMed ID: 24383149
[TBL] [Abstract][Full Text] [Related]
15. Medical devices; exemption from premarket notification; class II devices; wheelchair elevator. Final order.
Food and Drug Administration, HHS
Fed Regist; 2013 Mar; 78(42):14013-5. PubMed ID: 23476998
[TBL] [Abstract][Full Text] [Related]
16. Cardiovascular and neurological devices; reclassification of two embolization devices. Final rule.
Food and Drug Administration, HHS
Fed Regist; 2004 Dec; 69(249):77898-900. PubMed ID: 15624254
[TBL] [Abstract][Full Text] [Related]
17. Medical devices; reclassification of three anesthesiology preamendments class III devices into class II. Final rule.
Food and Drug Administration, HHS
Fed Regist; 2001 Nov; 66(221):57366-8. PubMed ID: 11776278
[TBL] [Abstract][Full Text] [Related]
18. Medical devices; ophthalmic devices; classification of the eyelid weight. Final rule.
Food and Drug Administration, HHS
Fed Regist; 2014 Apr; 79(76):22012-6. PubMed ID: 24754095
[TBL] [Abstract][Full Text] [Related]
19. Medical devices; exemption from premarket notification; class II devices; powered patient transport. Final order.
Food and Drug Administration, HHS
Fed Regist; 2013 Mar; 78(42):14015-7. PubMed ID: 23476999
[TBL] [Abstract][Full Text] [Related]
20. Cardiovascular devices; reclassification of external counter-pulsating devices for treatment of chronic stable angina; effective date of requirement for premarket approval for external counter-pulsating devices for other specified intended uses. Final order.
Food and Drug Administration, HHS
Fed Regist; 2013 Dec; 78(250):79304-8. PubMed ID: 24383148
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
