FDA 510(k) Applications Submitted by ARCADIA MEDICAL CORPORATION
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K031553 | 05/19/2003 | SILICONE FOAM CUFF TRACHEOSTOMY TUBES, SILICONE CUFFLESS NEONATAL AND PEDIATRIC TRACHEOSTOMY TUBES | ARCADIA MEDICAL CORPORATION |
| K060094 | 01/12/2006 | ARCADIA MEDICAL SILICONE WIRE REINFORCED ENDOTRACHEAL TUBES | ARCADIA MEDICAL CORPORATION |
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