Koven and Assoc., Inc.
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) | K922669 | MULTIDOP MODEL HD-2020 BI-DIRECTIONAL BLOOD FLOW | DPW | 1993-01-29 | View |
| 510(k) | K920333 | SMARTDOP 20 BI-DIRECTIONAL BLOOD FLOW DETECTOR | DPW | 1993-01-22 | View |
| 510(k) | K915550 | MINI DOPPLER II ULTRASOUND BLOOD FLOW DETECTOR | DPW | 1992-12-10 | View |
| 510(k) | K913595 | DS-240 AMBULATORY BLOOD PRESSURE MONITORING SYSTEM | DXN | 1992-03-27 | View |
| 510(k) | K912409 | MODEL HD-207 BIDIRECTIONAL VELOCITY METER | JOP | 1991-12-23 | View |
| 510(k) | K903026 | ES-1000SP II SMART DOP | DPW | 1991-02-26 | View |
| 510(k) | K894892 | HD-2200 PNEUMO-DOP VASCULAR TESTING SYSTEM | DSB | 1989-10-27 | View |
| 510(k) | K892707 | DVM-4200 BLOOD FLOWMETER | DPW | 1989-07-28 | View |
No matching devices.
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