The following data is part of a premarket notification filed by Coloplast A/s with the FDA for Comfeel Wound Dressing Ord.
Device ID | K922461 |
510k Number | K922461 |
Device Name: | COMFEEL WOUND DRESSING ORD |
Classification | Bandage, Liquid |
Applicant | COLOPLAST A/S WATER GARDENS PLACE SUITE 320 100 EAST 15TH ST. Ft. Worth, TX 76102 |
Contact | Richard A Hamer |
Correspondent | Richard A Hamer COLOPLAST A/S WATER GARDENS PLACE SUITE 320 100 EAST 15TH ST. Ft. Worth, TX 76102 |
Product Code | KMF |
CFR Regulation Number | 880.5090 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-05-26 |
Decision Date | 1992-08-17 |