Biofire Diagnostics
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) | K263054 | BIOFIRE Respiratory Panel 2.1 (RP2.1) | QOF | 2026-09-22 | View |
| 510(k) | K213954 | BIOFIRE SPOTFIRE Respiratory (R) Panel | QOF | 2023-02-03 | View |
No matching devices.
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