Agilent Technologies
FDA 510(k) & PMA Approved Devices — 13 products
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Total Devices13
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K010949 | 2010 PLUS HOLTER FOR WINDOWS | MLO | 2001-09-28 | View |
| 510(k) | K003940 | 2010 PLUS HOLTER FOR WINDOWS | MLO | 2001-02-08 | View |
| 510(k) | K003763 | 2010 PLUS HOLTER FOR WINDOWS | MLO | 2001-01-05 | View |
| 510(k) | K001308 | MODIFICATION TO ZYMED TELEMETRY SYSTEM, MODEL EASIVIEW | DQA | 2000-05-17 | View |
| 510(k) | K990093 | ZYMED TELEMETRY SYSTEM: MODEL EASIVIEW | DSI | 1999-05-11 | View |
| 510(k) | K980186 | ZYMED TELEMETRY SYSTEM | DSI | 1998-10-07 | View |
| 510(k) | K942781 | DIGITAL HOLTER RECORDER | DSH | 1995-01-24 | View |
| 510(k) | K930806 | ZYMED HOLTER SCANNER MODEL 2010 | DQK | 1994-04-25 | View |
| 510(k) | K924672 | ZYMED TELEMETRY MONITOR MODEL T8010 (PRELIMINARY) | DSI | 1992-12-15 | View |
| 510(k) | K895208 | ZYMED MODEL 1610 | DSI | 1989-12-12 | View |
| 510(k) | K841083 | QUIKPAGE ARRHYTHMIA REPORT GENERATOR | DSI | 1985-02-07 | View |
| 510(k) | K822970 | HOLTER RECORDER | DSH | 1982-11-03 | View |
| 510(k) | K822582 | QUIKPAGE SCANNER | DPS | 1982-09-21 | View |
No matching devices.
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