FDA 510(k) Applications Submitted by JOSEPHUS JANSSEN
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K131080 | 03/25/2013 | PHYSIOLASER OLYMPIC, SINGLE PROBES CW, CLUSTER PROBES CW, LIGHT NEEDLE, PHOTONIC SATELLITE | REIMERS AND JANSSEN GMBH |
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