FDA 510(k) Application Details - K960359

Device Classification Name	Mixer, Breathing Gases, Anesthesia Inhalation   More FDA Info for this Device
510(K) Number	K960359
Device Name	Mixer, Breathing Gases, Anesthesia Inhalation
Applicant	HAMILTON MEDICAL, INC. P.O. BOX 30008 RENO, NV 89520 US Other 510(k) Applications for this Company
Contact	TIM COWART Other 510(k) Applications for this Contact
Regulation Number	868.5330   More FDA Info for this Regulation Number
Classification Product Code	BZR Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/25/1996
Decision Date	04/24/1996
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