FDA 510(k) Application Details - K141928

Device Classification Name Calibrators, Drug Mixture

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510(K) Number K141928
Device Name Calibrators, Drug Mixture
Applicant Roche Diagnostics Operations (RDO)
9115 Hague Road
Indianapolis, IN 46250 US
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Contact NOEL K MENCIAS
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Regulation Number 862.3200

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Classification Product Code DKB
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Date Received 07/16/2014
Decision Date 11/25/2014
Decision SESE - SUBST EQUIV
Classification Advisory Committee TX - Clinical Toxicology
Review Advisory Committee CH - Clinical Chemistry
Statement / Summary / Purged Status Summary
Type Traditional
Reviewed By Third Party N
Expedited Review



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