The following data is part of a premarket notification filed by United States Surgical, A Division Of Tyco Healthc with the FDA for Manual Surgical Instrument For General Use.
| Device ID | K951173 |
| 510k Number | K951173 |
| Device Name: | MANUAL SURGICAL INSTRUMENT FOR GENERAL USE |
| Classification | Laparoscope, General & Plastic Surgery |
| Applicant | UNITED STATES SURGICAL, A DIVISION OF TYCO HEALTHC 150 GLOVER AVE. Norwalk, CT 06856 |
| Contact | Victor Clavelli |
| Correspondent | Victor Clavelli UNITED STATES SURGICAL, A DIVISION OF TYCO HEALTHC 150 GLOVER AVE. Norwalk, CT 06856 |
| Product Code | GCJ |
| CFR Regulation Number | 876.1500 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-03-15 |
| Decision Date | 1995-03-24 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 10884521180642 | K951173 | 000 |
| 10884521177000 | K951173 | 000 |