Intricon Datrix Corporation
FDA 510(k) & PMA Approved Devices — 2 products
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Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K112601 | INTRICON DATRIX SIRONA EVENT/ HOLTER RECORDER | MWJ | 2011-11-09 | View |
| 510(k) | K111160 | INTRICON DATRIX CENTAURI MT AMBULATORY PATIENT ECG TELEMETRY SYSTEM (APETS) | DSI | 2011-08-01 | View |
No matching devices.
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