The following data is part of a premarket notification filed by Amerx Health Care Corp. with the FDA for Amerigel Ointment.
Device ID | K970133 |
510k Number | K970133 |
Device Name: | AMERIGEL OINTMENT |
Classification | Dressing, Wound And Burn, Hydrogel W/drug And/or Biologic |
Applicant | AMERX HEALTH CARE CORP. 1150 CLEVELAND ST. SUITE 410 Clearwater, FL 34615 |
Contact | Ronald L Maddix |
Correspondent | Ronald L Maddix AMERX HEALTH CARE CORP. 1150 CLEVELAND ST. SUITE 410 Clearwater, FL 34615 |
Product Code | MGQ |
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 | 1997-01-15 |
Decision Date | 1997-04-14 |