Arcadia Medical Corporation
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) | K060094 | ARCADIA MEDICAL SILICONE WIRE REINFORCED ENDOTRACHEAL TUBES | BTR | 2006-05-08 | View |
| 510(k) | K031553 | SILICONE FOAM CUFF TRACHEOSTOMY TUBES, SILICONE CUFFLESS NEONATAL AND PEDIATRIC TRACHEOSTOMY TUBES | BTO | 2003-11-18 | View |
No matching devices.
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