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FDA 510(k) Application Details - K070546
Device Classification Name
Control, Hemoglobin
More FDA Info for this Device
510(K) Number
K070546
Device Name
Control, Hemoglobin
Applicant
Bio-Rad Laboratories
9500 JERONIMO RD.
IRVINE, CA 92618-2017 US
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Contact
ELIZABETH PLATT
Other 510(k) Applications for this Contact
Regulation Number
864.8625
More FDA Info for this Regulation Number
Classification Product Code
GGM
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More FDA Info for this Product Code
Date Received
02/26/2007
Decision Date
04/02/2007
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
HE - Hematology
Review Advisory Committee
CH - Clinical Chemistry
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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