Microphage, 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) | K120563 | KEYPATH MRSA/MSSA BLOOD CULTURE TEST-BT | OUS | 2012-03-30 | View |
| 510(k) | K102342 | KEYPATH(TM) MRSA/MSSA BLOOD CULTURE TEST- BT | OUS | 2011-05-05 | View |
No matching devices.
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