FDA 510(k) Application Details - K992192

Device Classification Name	Ventilator, Non-Continuous (Respirator)   More FDA Info for this Device
510(K) Number	K992192
Device Name	Ventilator, Non-Continuous (Respirator)
Applicant	TIARA MEDICAL SYSTEMS, INC. 14414 DETROIT AVE, SUITE 205 LAKEWOOD, OH 44107 US Other 510(k) Applications for this Company
Contact	GEOFFREY SLEEPER Other 510(k) Applications for this Contact
Regulation Number	868.5905   More FDA Info for this Regulation Number
Classification Product Code	BZD Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/29/1999
Decision Date	05/12/2000
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