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 Endoscopic Mini-retractor.
Device ID | K920068 |
510k Number | K920068 |
Device Name: | AUTO SUTURE ENDOSCOPIC MINI-RETRACTOR |
Classification | Laparoscope, General & Plastic Surgery |
Applicant | UNITED STATES SURGICAL, A DIVISION OF TYCO HEALTHC 150 GLOVER AVE. Norwalk, CT 06856 |
Contact | Nada Maric |
Correspondent | Nada Maric UNITED STATES SURGICAL, A DIVISION OF TYCO HEALTHC 150 GLOVER AVE. Norwalk, CT 06856 |
Product Code | GCJ |
CFR Regulation Number | 876.1500 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-01-07 |
Decision Date | 1992-09-17 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
20884523000808 | K920068 | 000 |
20884523000853 | K920068 | 000 |