FDA 510(k) Application Details - K012157

Device Classification Name	Stopcock, I.V. Set   More FDA Info for this Device
510(K) Number	K012157
Device Name	Stopcock, I.V. Set
Applicant	CHURCHILL MEDICAL SYSTEMS, INC. 87 VENTURE DR. DOVER, NH 03820 US Other 510(k) Applications for this Company
Contact	KEITH PALUCH Other 510(k) Applications for this Contact
Regulation Number	880.5440   More FDA Info for this Regulation Number
Classification Product Code	FMG Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/11/2001
Decision Date	09/11/2001
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review