AVD INTIMAX OCCLUSION CATHETER

Occluder, Catheter Tip

APPLIED VASCULAR DEVICES, INC.

The following data is part of a premarket notification filed by Applied Vascular Devices, Inc. with the FDA for Avd Intimax Occlusion Catheter.

Pre-market Notification Details

Device IDK910339
510k NumberK910339
Device Name:AVD INTIMAX OCCLUSION CATHETER
ClassificationOccluder, Catheter Tip
Applicant APPLIED VASCULAR DEVICES, INC. 26051 MERIT CIRCLE, #104 Laguna Hills,  CA  92653
ContactJo Stegwell
CorrespondentJo Stegwell
APPLIED VASCULAR DEVICES, INC. 26051 MERIT CIRCLE, #104 Laguna Hills,  CA  92653
Product CodeDQT  
CFR Regulation Number870.1370 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1991-01-28
Decision Date1991-05-29

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