The following data is part of a premarket notification filed by Invotec International, Inc. with the FDA for Invotec Clean Pad.
Device ID | K973580 |
510k Number | K973580 |
Device Name: | INVOTEC CLEAN PAD |
Classification | Gauze/sponge, Internal |
Applicant | INVOTEC INTERNATIONAL, INC. 11243-1 ST. JOHNS INDUSTRIAL PKWY. SOUTH Jacksonville, FL 32246 |
Contact | Jeffrey L Aull |
Correspondent | Jeffrey L Aull INVOTEC INTERNATIONAL, INC. 11243-1 ST. JOHNS INDUSTRIAL PKWY. SOUTH Jacksonville, FL 32246 |
Product Code | EFQ |
CFR Regulation Number | 510(k) Premarket Notification [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1997-09-19 |
Decision Date | 1997-12-10 |