5F MEDTRONIC LAUNCHER GUIDE CATHETER

Catheter, Percutaneous

MEDTRONIC VASCULAR

The following data is part of a premarket notification filed by Medtronic Vascular with the FDA for 5f Medtronic Launcher Guide Catheter.

Pre-market Notification Details

Device IDK030779
510k NumberK030779
Device Name:5F MEDTRONIC LAUNCHER GUIDE CATHETER
ClassificationCatheter, Percutaneous
Applicant MEDTRONIC VASCULAR 37A CHERRY HILL DR. Danvers,  MA  01923
ContactFred L Boucher
CorrespondentFred L Boucher
MEDTRONIC VASCULAR 37A CHERRY HILL DR. Danvers,  MA  01923
Product CodeDQY  
CFR Regulation Number870.1250 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeSpecial
3rd Party ReviewedNo
Combination ProductNo
Date Received2003-03-11
Decision Date2003-04-24
Summary:summary

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