Pathwork Diagnostics, Inc.
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) | K120489 | TISSUE OF ORIGIN TEST KIT FFPE | OIW | 2012-05-17 | View |
| 510(k) | K080896 | PATHWORK DIAGNOSTICS TISSUE OF ORIGIN TEST | OIW | 2008-07-30 | View |
No matching devices.
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