D.R.G.
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) | K890126 | KAMED STETHOSCOPE | LDE | 1989-04-21 | View |
| 510(k) | K844184 | D300 PORT ULTRASOUND LIN SCAN W/3.5 & 5.0 MHZ PROB | IYO | 1985-09-06 | View |
No matching devices.
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