MEDISTIM VERIQC SYSTEM

Flowmeter, Blood, Cardiovascular

MEDI-STIM ASA

The following data is part of a premarket notification filed by Medi-stim Asa with the FDA for Medistim Veriqc System.

Pre-market Notification Details

Device IDK102595
510k NumberK102595
Device Name:MEDISTIM VERIQC SYSTEM
ClassificationFlowmeter, Blood, Cardiovascular
Applicant MEDI-STIM ASA 435 RICE CREEK TERRACE NE Fridley,  MN  55432
ContactConstance G Bundy
CorrespondentConstance G Bundy
MEDI-STIM ASA 435 RICE CREEK TERRACE NE Fridley,  MN  55432
Product CodeDPW  
Subsequent Product CodeITX
Subsequent Product CodeIYN
Subsequent Product CodeIYO
CFR Regulation Number870.2100 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2010-09-09
Decision Date2010-12-27
Summary:summary

NIH GUDID Devices

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