ClearanceBrief
510(k) K982031 ยท GEX Powered Laser Surgical Instrument

OCULIGHT GL WITH THE DERMATOLOGY HANDPIECE

ApplicantIridex Corp, Mountain View CA, US
DecisionSubstantially Equivalent, Sep 8, 1998
ReceivedJun 10, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K982031

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.