FDA 510(k) Application Details - K952083

Device Classification Name	Vaporizer, Anesthesia, Non-Heated   More FDA Info for this Device
510(K) Number	K952083
Device Name	Vaporizer, Anesthesia, Non-Heated
Applicant	CLOVER MEDICAL EQUIPMENT SERVICES, INC. 172 HOLTZ DR. BUFFALO, NY 14225 US Other 510(k) Applications for this Company
Contact	RONALD LUICH Other 510(k) Applications for this Contact
Regulation Number	868.5880   More FDA Info for this Regulation Number
Classification Product Code	CAD Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/03/1995
Decision Date	10/21/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review