The following data is part of a premarket notification filed by Johnson & Johnson Medical, Ltd. with the FDA for Promogran Matrix Wound Dressing.
Device ID | K014129 |
510k Number | K014129 |
Device Name: | PROMOGRAN MATRIX WOUND DRESSING |
Classification | Dressing, Wound, Drug |
Applicant | JOHNSON & JOHNSON MEDICAL, LTD. ROUTE 22 WEST P.O. BOX 151 Somerville, NJ 08876 |
Contact | Sergio J Gadaleta |
Correspondent | Sergio J Gadaleta JOHNSON & JOHNSON MEDICAL, LTD. ROUTE 22 WEST P.O. BOX 151 Somerville, NJ 08876 |
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 | 2001-12-17 |
Decision Date | 2002-02-14 |
Summary: | summary |