The following data is part of a premarket notification filed by Convatec, A Division Of E.r. Squibb & Sons with the FDA for Duoderm Flexible Hydroactive Dressings.
Device ID | K841287 |
510k Number | K841287 |
Device Name: | DUODERM FLEXIBLE HYDROACTIVE DRESSINGS |
Classification | Dressing, Wound, Drug |
Applicant | CONVATEC, A DIVISION OF E.R. SQUIBB & SONS 4221 Richmond Rd., N.W. Walker, MI 49534 |
Product Code | FRO |
CFR Regulation Number | 510(k) Premarket Notification [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1984-03-28 |
Decision Date | 1984-08-20 |