The following data is part of a premarket notification filed by Advanced Surgical, Inc. with the FDA for Surgical Retractor Kit.
Device ID | K940193 |
510k Number | K940193 |
Device Name: | SURGICAL RETRACTOR KIT |
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 | 1994-01-13 |
Decision Date | 1994-02-15 |