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FDA 510(k) Applications for Medical Device Product Code "DRI"
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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 |