FDA 510(k) Application Details - K990132

Device Classification Name	Vaporizer, Anesthesia, Non-Heated   More FDA Info for this Device
510(K) Number	K990132
Device Name	Vaporizer, Anesthesia, Non-Heated
Applicant	DATEX-OHMEDA, INC. P.O. BOX 7550 MADISON, WI 53707 US Other 510(k) Applications for this Company
Contact	DANIEL KOSEDNAR 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	01/14/1999
Decision Date	01/21/1999
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review