FDA 510(k) Application Details - K955345

Device Classification Name	Cryptosporidium Spp.   More FDA Info for this Device
510(K) Number	K955345
Device Name	Cryptosporidium Spp.
Applicant	LMD LABORATORIES 2792 LOKER AVE., WEST, #103 SUITE 103 CARLSBAD, CA 92008 US Other 510(k) Applications for this Company
Contact	DAVID N LAMBILLOTTE Other 510(k) Applications for this Contact
Regulation Number	866.3220   More FDA Info for this Regulation Number
Classification Product Code	MHJ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/21/1995
Decision Date	06/07/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	MI - Microbiology
Review Advisory Committee	MI - Microbiology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review