Rohe Scientific Corp.
FDA 510(k) & PMA Approved Devices — 2 products
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Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K810038 | DIGITAL DIAGNOSTIC ULTRASOUND DEVICE | IYO | 1981-04-17 | View |
| 510(k) | K770073 | PRIMUS INTER PARESECHOCARDIOGRAPHY SYS. | DXK | 1977-01-25 | View |
No matching devices.
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