The following data is part of a premarket notification filed by Minumys Surgical, Inc. with the FDA for Slimline Surgical Clamp; Slimline Jaw Inserts.
| Device ID | K992640 |
| 510k Number | K992640 |
| Device Name: | SLIMLINE SURGICAL CLAMP; SLIMLINE JAW INSERTS |
| Classification | Clamp, Vascular |
| Applicant | MINUMYS SURGICAL, INC. 10231 BUBB RD. Cupertino, CA 95014 |
| Contact | Noel Messenger |
| Correspondent | Noel Messenger MINUMYS SURGICAL, INC. 10231 BUBB RD. Cupertino, CA 95014 |
| Product Code | DXC |
| CFR Regulation Number | 870.4450 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1999-08-06 |
| Decision Date | 1999-09-08 |
| Summary: | summary |