Canberra Industries, Inc.
FDA 510(k) & PMA Approved Devices — 3 products
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Total Devices3
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K925265 | IMAGEVIEW 46000 | LMC | 1993-06-09 | View |
| 510(k) | K896202 | MATRIX(TM)-96 | JJJ | 1990-01-02 | View |
| 510(k) | K834168 | FIBRINOGEN UPTAKE SYS -VARIOUS MODELS | JZD | 1983-12-29 | View |
No matching devices.
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