Remco Italia S.P.A.
FDA 510(k) & PMA Approved Devices — 3 products
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Total Devices3
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K032200 | ELAN DIGITAL 12 CHANNEL ELECTROCARDIOGRAPH | DPS | 2003-10-03 | View |
| 510(k) | K032276 | CLICK HOLTER | MWJ | 2003-08-27 | View |
| 510(k) | K852770 | CARIOLINE(ELECTROCARDIOGRAPH) | DPS | 1985-08-01 | View |
No matching devices.
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