Pertrach
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) | K914743 | EMERGENCY PERCUTANEOUS CRICOTHYROIDOTOMY KIT,MODIF | BTO | 1992-07-10 | View |
| 510(k) | K885139 | MODIFIED ADULT CRICOTHYROIDOTOMY KIT | BTO | 1989-05-25 | View |
No matching devices.
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