The following data is part of a premarket notification filed by Thomasville Medical Assoc. with the FDA for Vaginal Specula: Cusco, Guttman, Infant.
Device ID | K926429 |
510k Number | K926429 |
Device Name: | VAGINAL SPECULA: CUSCO, GUTTMAN, INFANT |
Classification | Speculum, Vaginal, Metal |
Applicant | THOMASVILLE MEDICAL ASSOC. 935 COBBLESTONE COURT Alpharetta, GA 30201 |
Contact | Thomas J Zinnanti |
Correspondent | Thomas J Zinnanti THOMASVILLE MEDICAL ASSOC. 935 COBBLESTONE COURT Alpharetta, GA 30201 |
Product Code | HDF |
CFR Regulation Number | 884.4520 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-12-23 |
Decision Date | 1994-02-28 |