SPECIMEN REMOVAL DEVICE

Laparoscope, General & Plastic Surgery

GENERAL SURGICAL INNOVATIONS

The following data is part of a premarket notification filed by General Surgical Innovations with the FDA for Specimen Removal Device.

Pre-market Notification Details

Device IDK941249
510k NumberK941249
Device Name:SPECIMEN REMOVAL DEVICE
ClassificationLaparoscope, General & Plastic Surgery
Applicant GENERAL SURGICAL INNOVATIONS 3278 ALPINE RD. Portola Valley,  CA  94028
ContactThomas J Fogarty
CorrespondentThomas J Fogarty
GENERAL SURGICAL INNOVATIONS 3278 ALPINE RD. Portola Valley,  CA  94028
Product CodeGCJ  
CFR Regulation Number876.1500 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1994-03-15
Decision Date1994-07-07

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.