FDA 510(k) Application Details - K942210

Device Classification Name	Ventilator, Continuous, Non-Life-Supporting   More FDA Info for this Device
510(K) Number	K942210
Device Name	Ventilator, Continuous, Non-Life-Supporting
Applicant	PURITAN BENNETT CORP. 10800 PFLUMM RD. LENEXA, KS 66215 US Other 510(k) Applications for this Company
Contact	C. MARSHALL SMITH Other 510(k) Applications for this Contact
Regulation Number	868.5895   More FDA Info for this Regulation Number
Classification Product Code	MNS Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/03/1994
Decision Date	02/09/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review