ORIGIN FLEXIBLE PORT

Laparoscope, General & Plastic Surgery

ORIGIN MEDSYSTEMS, INC.

The following data is part of a premarket notification filed by Origin Medsystems, Inc. with the FDA for Origin Flexible Port.

Pre-market Notification Details

Device IDK922751
510k NumberK922751
Device Name:ORIGIN FLEXIBLE PORT
ClassificationLaparoscope, General & Plastic Surgery
Applicant ORIGIN MEDSYSTEMS, INC. 1021 HOWARD AVE. San Carlos,  CA  94070
ContactAlbert K Chin
CorrespondentAlbert K Chin
ORIGIN MEDSYSTEMS, INC. 1021 HOWARD AVE. San Carlos,  CA  94070
Product CodeGCJ  
CFR Regulation Number876.1500 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1992-06-08
Decision Date1992-11-20

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