FDA 510(k) Applications Submitted by REIMERS AND JANSSEN GMBH

FDA 510(k) Number Submission Date Device Name Applicant
K091675 06/09/2009 LASERPEN PRACTISE AND EXPERT, HANDYLASER SPRINT, HANDYLASER TRION, PHYSIOLASER OLYMPIC, POLYLASER REIMERS AND JANSSEN GMBH
K131080 03/25/2013 PHYSIOLASER OLYMPIC, SINGLE PROBES CW, CLUSTER PROBES CW, LIGHT NEEDLE, PHOTONIC SATELLITE REIMERS AND JANSSEN GMBH


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