The following data is part of a premarket notification filed by Advanced Surgical, Inc. with the FDA for Knot Pusher.
| Device ID | K933243 |
| 510k Number | K933243 |
| Device Name: | KNOT PUSHER |
| Classification | Laparoscope, General & Plastic Surgery |
| Applicant | ADVANCED SURGICAL, INC. 305 COLLEGE RD. EAST Princeton, NJ 08540 |
| Contact | Angelique Layton Anderson |
| Correspondent | Angelique Layton Anderson ADVANCED SURGICAL, INC. 305 COLLEGE RD. EAST Princeton, NJ 08540 |
| Product Code | GCJ |
| CFR Regulation Number | 876.1500 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-07-02 |
| Decision Date | 1993-10-21 |