ClearanceBrief
510(k) K930582 ยท GEX Powered Laser Surgical Instrument

SHARPLAN SHARPLASE LATERAL ND:YAG FIBER

ApplicantSharplan Lasers, Inc., Allendale NJ, US
DecisionSubstantially Equivalent, Nov 2, 1993
ReceivedFeb 4, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K930582

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.