Remote Diagnostic Technologies , Ltd.
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) | K173768 | Tempus Pro Patient Monitor | MHX | 2018-01-10 | View |
| 510(k) | K170567 | Tempus Pro Patient Monitor | MHX | 2017-07-06 | View |
| 510(k) | K130773 | TEMPUS PRO PATIENT MONITOR | MWI | 2013-06-05 | View |
| 510(k) | K113105 | TEMPUSIC PATIENT MONITOR | MWI | 2011-12-15 | View |
| 510(k) | K101264 | TEMPUS IC PROFESSIONAL PATIENT MONITOR | MWI | 2010-05-11 | View |
| 510(k) | K082718 | TEMPUSIC PATIENT MONITOR | DXH | 2008-10-10 | View |
| 510(k) | K033410 | TEMPUS 2000 PATIENT MONITOR, MODEL 00-0002 | DXH | 2004-03-05 | View |
| 510(k) | K010436 | TEMPUS 2000 PATIENT MONITOR, MODEL 00-0001; TEMPUS MONITORING STATION, MODEL 01-0011 | DXH | 2001-05-14 | View |
No matching devices.
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