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 |