FDA 510(k) Applications for Medical Device Product Code: DRI (Monitor, Line Isolation)

FDA 510(k) Applications for Medical Device Product Code "DRI"
(Monitor, Line Isolation)

FDA 510(k) Number	Applicant	Device Name	Decision Date
K902493	DATEX DIVISION INSTRUMENTARIUM CORP.	CARDIOCAP II CG-2GS, 2G, 1GS, 1G, 2CG, CS MONITOR	07/06/1990
K902492	DATEX DIVISION INSTRUMENTARIUM CORP.	CARDIOCAP II MONITORS: CH, CH-2, CH-S, CH-2S	07/06/1990
K822316	HMBA	HEART MONITOR BRACELET ALARM	09/21/1982
K802326	STANCO MEDICAL, INC.	PRESSURE MONITORING LINES	10/10/1980