FDA 510(k) Application Details - K962859

Device Classification Name	Station, Pipetting And Diluting, For Clinical Use   More FDA Info for this Device
510(K) Number	K962859
Device Name	Station, Pipetting And Diluting, For Clinical Use
Applicant	CAVRO SCIENTIFIC INSTRUMENTS, INC. 242 HUMBOLDT CT. SUNNYVALE, CA 94089 US Other 510(k) Applications for this Company
Contact	FRED WOLCOTT Other 510(k) Applications for this Contact
Regulation Number	862.2750   More FDA Info for this Regulation Number
Classification Product Code	JQW Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/22/1996
Decision Date	10/29/1996
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