The following data is part of a premarket notification filed by Zinnanti Surgical Instruments, Inc. with the FDA for Biopsy Forceps.
| Device ID | K892252 |
| 510k Number | K892252 |
| Device Name: | BIOPSY FORCEPS |
| Classification | Forceps, Biopsy, Non-electric |
| Applicant | ZINNANTI SURGICAL INSTRUMENTS, INC. 21540-B PRAIRIE ST. Chatsworth, CA 91311 |
| Contact | Anthony Zinnanti |
| Correspondent | Anthony Zinnanti ZINNANTI SURGICAL INSTRUMENTS, INC. 21540-B PRAIRIE ST. Chatsworth, CA 91311 |
| Product Code | FCL |
| CFR Regulation Number | 876.1075 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1989-04-04 |
| Decision Date | 1989-10-03 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| G373144005J0 | K892252 | 000 |