Echocath, Inc.
FDA 510(k) & PMA Approved Devices — 6 products
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Total Devices6
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K010482 | ECHOFLOW PORTABLE DOPPLER BLOOD FLOW MEASUREMENT SYSTEM; MODEL PEF-1 | JOP | 2001-03-20 | View |
| 510(k) | K990642 | ECHOFLOW DOPPLER BLOOD VELOCITY METER | JOP | 1999-09-16 | View |
| 510(k) | K932436 | ECHOMARK INTRAUTERINE GUIDING CATHETER | MOV | 1995-11-16 | View |
| 510(k) | K933417 | ECHOMARK(R) ELECTROPHYSIOLOGY CATHETER | DRF | 1995-05-04 | View |
| 510(k) | K926351 | COLORMARK(TM) VISUALIZATION SYSTEM | IYN | 1993-09-16 | View |
| 510(k) | K922787 | ECHOMARK GUIDEWIRE WITH ULTRASONIC LOCALIZATION | DQX | 1993-01-06 | View |
No matching devices.
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