HEMOSIL HIGH ABNORMAL CONTROL ASSAYED

Plasma, Coagulation Control

INSTRUMENTATION LABORATORY CO.

The following data is part of a premarket notification filed by Instrumentation Laboratory Co. with the FDA for Hemosil High Abnormal Control Assayed.

Pre-market Notification Details

Device IDK021024
510k NumberK021024
Device Name:HEMOSIL HIGH ABNORMAL CONTROL ASSAYED
ClassificationPlasma, Coagulation Control
Applicant INSTRUMENTATION LABORATORY CO. 180 HARTWELL ROAD Bedford,  MA  01730
ContactCarol Marble
CorrespondentCarol Marble
INSTRUMENTATION LABORATORY CO. 180 HARTWELL ROAD Bedford,  MA  01730
Product CodeGGN  
CFR Regulation Number864.5425 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2002-03-29
Decision Date2002-05-16
Summary:summary

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
08426950660675 K021024 000
08426950078999 K021024 000

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