Biomecca Australia , Ltd.
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) | K860790 | BIOMECCA CARETAKER 1000 & 2000 | DPS | 1986-05-08 | View |
| 510(k) | K854639 | BIOMECCA CENTRAL CS1 | DRT | 1986-04-17 | View |
No matching devices.
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