The following data is part of a premarket notification filed by Arthropedics, Inc. with the FDA for Cup Biopsy Forceps, Left.
| Device ID | K873503 |
| 510k Number | K873503 |
| Device Name: | CUP BIOPSY FORCEPS, LEFT |
| Classification | Forceps |
| Applicant | ARTHROPEDICS, INC. 111 LESTER ST. Wallington, NJ 07057 |
| Contact | Jerry Procopio |
| Correspondent | Jerry Procopio ARTHROPEDICS, INC. 111 LESTER ST. Wallington, NJ 07057 |
| Product Code | HTD |
| CFR Regulation Number | 878.4800 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-08-31 |
| Decision Date | 1987-11-02 |