STRYKER ENDOSCOPIC INSTRUMENTS AND ACCESSORIES

Electrosurgical, Cutting & Coagulation & Accessories

Stryker Endoscopy

The following data is part of a premarket notification filed by Stryker Endoscopy with the FDA for Stryker Endoscopic Instruments And Accessories.

Pre-market Notification Details

Device IDK935237
510k NumberK935237
Device Name:STRYKER ENDOSCOPIC INSTRUMENTS AND ACCESSORIES
ClassificationElectrosurgical, Cutting & Coagulation & Accessories
Applicant Stryker Endoscopy 210 BAYPOINTE PKWY. San Jose,  CA  95134
ContactThomas Kelly
CorrespondentThomas Kelly
Stryker Endoscopy 210 BAYPOINTE PKWY. San Jose,  CA  95134
Product CodeGEI  
CFR Regulation Number878.4400 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1993-11-01
Decision Date1994-03-21

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
07613327060539 K935237 000
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07613327052329 K935237 000
07613327051407 K935237 000

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