Emergency Filtration Products, 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) | K012958 | BREATHING CIRCUIT FILTER | CAH | 2002-02-22 | View |
| 510(k) | K980052 | RESPAIDE | CBP | 1998-08-05 | View |
No matching devices.
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