Shiley Dispos. Decannulation Plug W/Sw/
by Shiley, Inc. 510(k)
Active Open recall
510(k) K843730
Regulatory status
Recall ongoing. 1 ongoing FDA recall names this device. See recalls
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK843730 | Date19 Oct 1984 | StatusActive |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Recalls
-
- Ongoing Z-2653-2026
Due to product labeling incorrectly including the symbol indicating non-DEHP (Bis(2-ethylhexyl) phthalate as the product includes 30 to 35% DEHP.
Specification
- 510(k) Number
- FDA Product Code
- BTO
- Device Class
- Class II
- Regulation
- 21 CFR Part 868.5800
- Advisory Committee
- Anesthesiology
- FDA Decision
- SESE Substantially Equivalent