FDA 510(k) Application Details - K983387

Device Classification Name Drug Mixture Control Materials

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510(K) Number K983387
Device Name Drug Mixture Control Materials
Applicant ROCHE DIAGNOSTIC SYSTEMS, INC.
BRANCHBURG TOWNSHIP
1080 U.S. HIGHWAY 202
SOMERVILLE, NJ 08876-3771 US
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Contact MARIA FEIJOO
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Regulation Number 862.3280

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Classification Product Code DIF
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Date Received 09/25/1998
Decision Date 10/09/1998
Decision SESE - SUBST EQUIV
Classification Advisory Committee TX - Clinical Toxicology
Review Advisory Committee CH - Clinical Chemistry
Statement / Summary / Purged Status Statement
Type Traditional
Reviewed By Third Party N
Expedited Review



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