FDA 510(k) Application Details - K013596

Device Classification Name System, Automated Platelet Aggregation

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510(K) Number K013596
Device Name System, Automated Platelet Aggregation
Applicant ACCUMETRICS, INC.
3985 SORRENTO VALLEY BLVD.
SAN DIEGO, CA 92121 US
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Contact RHONDA MOE
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Regulation Number 864.5700

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Classification Product Code JOZ
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Date Received 10/31/2001
Decision Date 05/16/2002
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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