FDA 510(k) Application Details - K150270

Device Classification Name	System, Test, Vitamin D   More FDA Info for this Device
510(K) Number	K150270
Device Name	System, Test, Vitamin D
Applicant	TOSOH BIOSCIENCE, INC. 6000 SHORELINE COURT SUITE 101 SOUTH SAN FRANCISCO, CA 94080 US Other 510(k) Applications for this Company
Contact	Robert L Wick Other 510(k) Applications for this Contact
Regulation Number	862.1825   More FDA Info for this Regulation Number
Classification Product Code	MRG Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/04/2015
Decision Date	10/26/2015
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
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