ClearanceBrief
510(k) K031800 ยท FTC Light, Ultraviolet, Dermatological

SOLARC/SOLRX 500 SERIES ULTRAVIOLET PHOTOTHERAPY LAMP UNIT FAMILY A NEW MEDICAL DEVICE FAMILY CONSISTING OF 5 MODELS:

ApplicantSolarc Systems, Inc., Barrie, Ontario, CA
DecisionSubstantially Equivalent, Sep 10, 2003
ReceivedJun 11, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K031800

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.