FDA 510(k) Application Details - K992571

Device Classification Name Activated Whole Blood Clotting Time

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510(K) Number K992571
Device Name Activated Whole Blood Clotting Time
Applicant I-STAT CORP.
104 WINDSOR CENTER DR.
EAST WINDSOR, NJ 08520 US
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Contact PAUL VANDERWERF
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Regulation Number 864.7140

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Classification Product Code JBP
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Date Received 08/02/1999
Decision Date 02/10/2000
Decision SESE - SUBST EQUIV
Classification Advisory Committee HE - Hematology
Review Advisory Committee HE - Hematology
Statement / Summary / Purged Status Summary
Type Traditional
Reviewed By Third Party N
Expedited Review



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