FDA 510(k) Applications Submitted by JOHN M MITCHELL
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K121398 | 05/09/2012 | CHARLIE GUIDEWIRE (REGULAR), CHARLIE GUIDEWIRE (STIFF) | GUIDEPATH MEDICAL, INC. |
| K993142 | 09/21/1999 | ELITE CUSTOM | SOMA BLUE, INC. |
| K993143 | 09/21/1999 | VITALITY SYSTEM | SOMA BLUE, INC. |
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