FDA 510(k) Application Details - K955940

Device Classification Name	Diazo Colorimetry, Bilirubin   More FDA Info for this Device
510(K) Number	K955940
Device Name	Diazo Colorimetry, Bilirubin
Applicant	DERMA MEDIA LAB., INC. 8531 WELLSFORD PL., SUITE E SANTA FE SPRINGS, CA 90670 US Other 510(k) Applications for this Company
Contact	CHARLES C ALLAIN Other 510(k) Applications for this Contact
Regulation Number	862.1110   More FDA Info for this Regulation Number
Classification Product Code	CIG Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/21/1995
Decision Date	03/13/1996
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