ACTIVE LIFE
Collector, Ostomy
CONVATEC, A DIVISION OF E.R. SQUIBB & SONS
The following data is part of a premarket notification filed by Convatec, A Division Of E.r. Squibb & Sons with the FDA for Active Life.
Pre-market Notification Details
| Device ID | K833625 |
| 510k Number | K833625 |
| Device Name: | ACTIVE LIFE |
| Classification | Collector, Ostomy |
| Applicant | CONVATEC, A DIVISION OF E.R. SQUIBB & SONS 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | EXB |
| CFR Regulation Number | 876.5900 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-10-14 |
| Decision Date | 1983-11-28 |
Trademark Results [ACTIVE LIFE]
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.