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FDA 510(k) Application Details - K955691
Device Classification Name
Multi-Analyte Controls, All Kinds (Assayed)
More FDA Info for this Device
510(K) Number
K955691
Device Name
Multi-Analyte Controls, All Kinds (Assayed)
Applicant
CLINICAL CONTROLS, INC.
750 FARROLL RD.
SUITE B
GROVER BEACH, CA 93433 US
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Contact
JAMES F GODFREY
Other 510(k) Applications for this Contact
Regulation Number
862.1660
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Classification Product Code
JJY
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More FDA Info for this Product Code
Date Received
12/14/1995
Decision Date
04/24/1996
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
CH - Clinical Chemistry
Review Advisory Committee
CH - Clinical Chemistry
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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