LEMAITRE EMBOLECTOMY CATHETER

Catheter, Embolectomy

VASCUTECH, INC.

The following data is part of a premarket notification filed by Vascutech, Inc. with the FDA for Lemaitre Embolectomy Catheter.

Pre-market Notification Details

Device IDK992368
510k NumberK992368
Device Name:LEMAITRE EMBOLECTOMY CATHETER
ClassificationCatheter, Embolectomy
Applicant VASCUTECH, INC. 164 MIDDLESEX TURNPIKE Burlington,  MA  01803
ContactTrent G Kamke
CorrespondentTrent G Kamke
VASCUTECH, INC. 164 MIDDLESEX TURNPIKE Burlington,  MA  01803
Product CodeDXE  
CFR Regulation Number870.5150 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1999-07-15
Decision Date1999-12-09

NIH GUDID Devices

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