The following data is part of a premarket notification filed by Laboratoires Urgo S.a. with the FDA for Algoplaque Hydrocolloid Dressing.
Device ID | K970518 |
510k Number | K970518 |
Device Name: | ALGOPLAQUE HYDROCOLLOID DRESSING |
Classification | Dressing, Wound And Burn, Occlusive |
Applicant | LABORATOIRES URGO S.A. 7527 WESTMORELAND AVE. St. Louis, MO 63105 |
Contact | Evan Dick, Ph.d. |
Correspondent | Evan Dick, Ph.d. LABORATOIRES URGO S.A. 7527 WESTMORELAND AVE. St. Louis, MO 63105 |
Product Code | MGP |
CFR Regulation Number | 510(k) Premarket Notification [🔎] |
Decision | Substantially Equivalent For Some Indications (SN) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1997-02-11 |
Decision Date | 1997-03-21 |