018 Hydrophilic Coated OTW PTA Balloon Dilatation Catheter

Catheter, Angioplasty, Peripheral, Transluminal

Creagh Medical, Ltd.

The following data is part of a premarket notification filed by Creagh Medical, Ltd. with the FDA for 018 Hydrophilic Coated Otw Pta Balloon Dilatation Catheter.

Pre-market Notification Details

Device IDK180007
510k NumberK180007
Device Name:018 Hydrophilic Coated OTW PTA Balloon Dilatation Catheter
ClassificationCatheter, Angioplasty, Peripheral, Transluminal
Applicant Creagh Medical, Ltd. IDA Business Park Ballinasloe,  IE H53 K8p4
ContactShane Costello
CorrespondentSherri Mellingen
dba Surmodics, Inc. 9924 West 74th Street Eden Prairie,  MN  55344
Product CodeLIT  
CFR Regulation Number870.1250 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2018-01-02
Decision Date2018-04-19
Summary:summary

NIH GUDID Devices

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