FDA 510(k) Applications Submitted by MARK FOOTE
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K060094 | 01/12/2006 | ARCADIA MEDICAL SILICONE WIRE REINFORCED ENDOTRACHEAL TUBES | ARCADIA MEDICAL CORPORATION |
Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact