The following data is part of a premarket notification filed by Thomasville Medical Assoc. with the FDA for Cannulated Biopsy Forceps.
Device ID | K926430 |
510k Number | K926430 |
Device Name: | CANNULATED BIOPSY FORCEPS |
Classification | Bronchoscope (flexible Or Rigid) |
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 | EOQ |
CFR Regulation Number | 874.4680 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-12-23 |
Decision Date | 1993-03-26 |