FDA 510(k) Applications Submitted by CHRIS LEWIS
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K140835 | 04/02/2014 | GENERAL AND PLASTIC SURGERY | SCION MEDICAL TECHNOLOGIES LLC |
| K053141 | 11/09/2005 | NEUROSIGN MOTOR NERVE MONITOR, MODELS NEUROSIGN 400 & 800 | THE MAGSTIM COMPANY LTD. |
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