FDA 510(k) Application Details - K000257

Device Classification Name	Acid Phosphatase (Prostatic), Tartrate Inhibited   More FDA Info for this Device
510(K) Number	K000257
Device Name	Acid Phosphatase (Prostatic), Tartrate Inhibited
Applicant	DIAGNOSTIC PRODUCTS CORP. 5700 WEST 96TH ST. LOS ANGELES, CA 90045-5597 US Other 510(k) Applications for this Company
Contact	EDWARD M LEVINE Other 510(k) Applications for this Contact
Regulation Number	862.1020   More FDA Info for this Regulation Number
Classification Product Code	JFH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/27/2000
Decision Date	02/23/2000
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CH - Clinical Chemistry
Review Advisory Committee	IM - Immunology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review