Esaote Biomedica Spa
FDA 510(k) & PMA Approved Devices — 4 products
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Total Devices4
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K933951 | VIDEO EEG OPTION MODIFICATION | GWQ | 1994-02-03 | View |
| 510(k) | K902368 | PERSONAL 120/210 BASIC ELECTROCARDIOGRAPH | DPS | 1990-09-11 | View |
| 510(k) | K896356 | AU530 DIAGNOSTIC ULTRASONIC PULSED ECHO SYSTEM | IYO | 1990-08-21 | View |
| 510(k) | K902334 | MONITOR, MODEL 2817 | DXJ | 1990-06-26 | View |
No matching devices.
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