The following data is part of a premarket notification filed by United States Surgical, A Division Of Tyco Healthc with the FDA for Minisite*bipolar Forceps** Device.
| Device ID | K972415 |
| 510k Number | K972415 |
| Device Name: | MINISITE*BIPOLAR FORCEPS** DEVICE |
| Classification | Electrosurgical, Cutting & Coagulation & Accessories |
| Applicant | UNITED STATES SURGICAL, A DIVISION OF TYCO HEALTHC 150 GLOVER AVE. Norwalk, CT 06856 |
| Contact | Melissa Mazzoni |
| Correspondent | Melissa Mazzoni UNITED STATES SURGICAL, A DIVISION OF TYCO HEALTHC 150 GLOVER AVE. Norwalk, CT 06856 |
| Product Code | GEI |
| CFR Regulation Number | 878.4400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1997-06-27 |
| Decision Date | 1997-09-19 |
| Summary: | summary |