Biosensor Corp.
FDA 510(k) & PMA Approved Devices — 10 products
Advertisement
Total Devices10
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K990956 | BIOSENSOR HOLTER MONITOR SYSTEM SOFTWARE, MODEL 1005 | DQK | 1999-06-14 | View |
| 510(k) | K974546 | BIOSENSOR HOLTER MONITOR SYSTEM | DQK | 1998-03-04 | View |
| 510(k) | K974192 | BIOSENSOR HOLTER MONITOR SYSTEM | DQK | 1998-03-04 | View |
| 510(k) | K950944 | AMBULATORY (HOLTER) RECORDING SYSTEM | DQK | 1996-06-18 | View |
| 510(k) | K960449 | PC ECG 1200 ECG AND STRESS ELECTROCARDIOGRAPHY TESTING SYSTEM(VERSION 2.90) | DPS | 1996-05-30 | View |
| 510(k) | K943338 | BIOSENSOR BIDOP VASCULAR TEST SYSTEM | JAF | 1996-04-12 | View |
| 510(k) | K950723 | AMBULATORY (HOLTER) RECORDING SYSTEM | DQK | 1996-02-09 | View |
| 510(k) | K922027 | AMBULATORY (HOLTER) RECORDING, MODIFICATION | DSI | 1993-02-17 | View |
| 510(k) | K895266 | AMBULATORY (HOLTER) RECORDING SYSTEM - MODIFIED | DSI | 1990-01-26 | View |
| 510(k) | K831676 | BIOSENSOR ASC SYSTEM | DSI | 1983-12-01 | View |
No matching devices.
Advertisement