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


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact