Cardiodata Corp.
FDA 510(k) & PMA Approved Devices — 4 products
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Total Devices4
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K900607 | MK5 DETECTOR & ALARM, ARRHYTHMIA W/SOFTWARE 2.11 | DSI | 1990-10-16 | View |
| 510(k) | K881488 | HOLTER SCANNER | DSI | 1988-09-20 | View |
| 510(k) | K873337 | MODEL SSR1 HOLTER MONITOR | DSH | 1987-10-09 | View |
| 510(k) | K860167 | PRODIGY AND PRODIGY PLUS | DSI | 1986-03-31 | View |
No matching devices.
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