ACTIVE-LIFE
Collector, Ostomy
E. R. SQUIBB & SONS, INC.
The following data is part of a premarket notification filed by E. R. Squibb & Sons, Inc. with the FDA for Active-life.
Pre-market Notification Details
| Device ID | K780454 |
| 510k Number | K780454 |
| Device Name: | ACTIVE-LIFE |
| Classification | Collector, Ostomy |
| Applicant | E. R. SQUIBB & SONS, INC. 40 W 57TH ST. New York, NY 10019 |
| Product Code | EXB |
| CFR Regulation Number | 876.5900 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1978-03-20 |
| Decision Date | 1978-04-21 |
Trademark Results [ACTIVE-LIFE]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 ACTIVE-LIFE 85532734 not registered Dead/Abandoned |
STOMAPLEX LLC 2012-02-02 |
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