Grandcor Medical Systems
FDA 510(k) & PMA Approved Devices — 8 products
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Total Devices8
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K905480 | SPIROSCOPE | BZC | 1991-05-06 | View |
| 510(k) | K895547 | GRANDCOR/CARDIOLINE ECT STRESS TESTING | DSI | 1990-03-13 | View |
| 510(k) | K883410 | CARDIOMEGA-T | DSI | 1988-10-17 | View |
| 510(k) | K871890 | CARDIO-MEGA SYSTEM | DSI | 1987-06-12 | View |
| 510(k) | K864260 | APPLICARD SYSTEM (ECG ELECTRODE SYSTEM) | DRX | 1987-05-11 | View |
| 510(k) | K864978 | APPLISCOPE | DPS | 1987-02-19 | View |
| 510(k) | K864581 | APPLIDYN | ISD | 1987-01-21 | View |
| 510(k) | K862375 | CARDIO PORT 500 24-H ECG AMBULATORY MONITOR SYSTEM | DSI | 1986-07-01 | View |
No matching devices.
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