The following data is part of a premarket notification filed by United States Surgical, A Division Of Tyco Healthc with the FDA for Nonpowered Neurosurgical Instrument.
| Device ID | K953173 |
| 510k Number | K953173 |
| Device Name: | NONPOWERED NEUROSURGICAL INSTRUMENT |
| Classification | Endoscope, Neurological |
| Applicant | UNITED STATES SURGICAL, A DIVISION OF TYCO HEALTHC 150 GLOVER AVE. Norwalk, CT 06856 |
| Contact | Janet G Johnson |
| Correspondent | Janet G Johnson UNITED STATES SURGICAL, A DIVISION OF TYCO HEALTHC 150 GLOVER AVE. Norwalk, CT 06856 |
| Product Code | GWG |
| CFR Regulation Number | 882.1480 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-07-07 |
| Decision Date | 1995-10-03 |