FDA 510(k) Applications Submitted by BRODIE PEDERSEN
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K140785 | 03/31/2014 | PULSE OXIMETER | NONIN MEDICAL, INC. |
| K131021 | 04/12/2013 | PULSE OXIMETER | NONIN MEDICAL, INC. |
| K132402 | 08/01/2013 | SENSMART MODEL X-100 UNIVERAL OXIMETRY SYSTEM | NONIN MEDICAL, INC. |
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