EPIVIEW
Dressing, Wound And Burn, Occlusive
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 Epiview.
Pre-market Notification Details
| Device ID | K961319 |
| 510k Number | K961319 |
| Device Name: | EPIVIEW |
| Classification | Dressing, Wound And Burn, Occlusive |
| Applicant | CONVATEC, A DIVISION OF E.R. SQUIBB & SONS 100 HEADQUARTERS PARK DR. Skillman, NJ 08558 |
| Contact | Adrenne Mcnally |
| Correspondent | Adrenne Mcnally CONVATEC, A DIVISION OF E.R. SQUIBB & SONS 100 HEADQUARTERS PARK DR. Skillman, NJ 08558 |
| Product Code | MGP |
| CFR Regulation Number | 510(k) Premarket Notification [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-04-05 |
| Decision Date | 1996-07-08 |
| Summary: | summary |
Trademark Results [EPIVIEW]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 EPIVIEW 77492448 not registered Dead/Abandoned |
Indigo-Orb Inc 2008-06-06 |
 EPIVIEW 75547257 2446783 Live/Registered |
VEECO INSTRUMENTS INC. 1998-09-02 |
 EPIVIEW 75101345 2090114 Dead/Cancelled |
E. R. SQUIBB & SONS, INC. 1996-05-09 |
 EPIVIEW 74323055 not registered Dead/Abandoned |
E. R. Squibb & Sons, Inc. 1992-10-16 |
 EPIVIEW 73837963 1599194 Dead/Cancelled |
E. R. SQUIBB & SONS, INC. 1989-11-13 |
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.