FDA 510(k) Application Details - K971182

Device Classification Name	Reagents, Clostridium Difficile Toxin   More FDA Info for this Device
510(K) Number	K971182
Device Name	Reagents, Clostridium Difficile Toxin
Applicant	TECHLAB, INC. 1861 PRATT DR. CORPORATE RESEARCH CENTER BLACKSBURG, VA 24060-6364 US Other 510(k) Applications for this Company
Contact	DAVID M LYERLY Other 510(k) Applications for this Contact
Regulation Number	866.2660   More FDA Info for this Regulation Number
Classification Product Code	LLH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/31/1997
Decision Date	07/22/1997
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