The following data is part of a premarket notification filed by United States Surgical, A Division Of Tyco Healthc with the FDA for Auto Suture(r) Endoscopic Clamp.
| Device ID | K903205 |
| 510k Number | K903205 |
| Device Name: | AUTO SUTURE(R) ENDOSCOPIC CLAMP |
| Classification | Forceps, Obstetrical |
| Applicant | UNITED STATES SURGICAL, A DIVISION OF TYCO HEALTHC 150 GLOVER AVE. Norwalk, CT 06856 |
| Contact | Steve Reitzler |
| Correspondent | Steve Reitzler UNITED STATES SURGICAL, A DIVISION OF TYCO HEALTHC 150 GLOVER AVE. Norwalk, CT 06856 |
| Product Code | HDA |
| CFR Regulation Number | 884.4400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1990-07-20 |
| Decision Date | 1990-10-11 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 20884523000839 | K903205 | 000 |
| 20884523000754 | K903205 | 000 |