FDA 510(k) Application Details - K981773

Device Classification Name	Vaporizer, Anesthesia, Non-Heated   More FDA Info for this Device
510(K) Number	K981773
Device Name	Vaporizer, Anesthesia, Non-Heated
Applicant	DRAEGER MEDICAL, INC. 3135 QUARRY RD. TELFORD, PA 18969 US Other 510(k) Applications for this Company
Contact	J. TERESA DORRIETY 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	05/20/1998
Decision Date	07/06/1998
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