FDA 510(k) Application Details - K142448

Device Classification Name

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510(K) Number K142448
Device Name VARIANT II TURBO HbA1c Kit - 2.0
Applicant Bio-Rad Laboratories, Inc.
4000 Alfred Nobel Dr.
Hercules, CA 94547 US
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Contact Jackie Buckley
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Regulation Number

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Classification Product Code PDJ
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Date Received 09/02/2014
Decision Date 03/24/2015
Decision SESE - SUBST EQUIV
Classification Advisory Committee CH - Clinical Chemistry
Review Advisory Committee CH - Clinical Chemistry
Statement / Summary / Purged Status Summary
Type Traditional
Reviewed By Third Party N
Expedited Review



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