AUTO SUTURE ENDOSCOPIC MINI-RETRACTOR

Laparoscope, General & Plastic Surgery

UNITED STATES SURGICAL, A DIVISION OF TYCO HEALTHC

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.

Pre-market Notification Details

Device IDK920068
510k NumberK920068
Device Name:AUTO SUTURE ENDOSCOPIC MINI-RETRACTOR
ClassificationLaparoscope, General & Plastic Surgery
Applicant UNITED STATES SURGICAL, A DIVISION OF TYCO HEALTHC 150 GLOVER AVE. Norwalk,  CT  06856
ContactNada Maric
CorrespondentNada Maric
UNITED STATES SURGICAL, A DIVISION OF TYCO HEALTHC 150 GLOVER AVE. Norwalk,  CT  06856
Product CodeGCJ  
CFR Regulation Number876.1500 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1992-01-07
Decision Date1992-09-17

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
20884523000808 K920068 000
20884523000853 K920068 000

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.