Avalon Technology 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) | K904317 | AVALON GENERAL PURPOSE SCANNER, PREVIEW GP | DPW | 1991-02-13 | View |
| 510(k) | K895359 | ADMS MULTIPLANE RECTAL PROBE | ITX | 1989-11-22 | View |
No matching devices.
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