ClearanceBrief
510(k) K961279 ยท GEX Powered Laser Surgical Instrument

SHARPLAN LASERS, INC. RUBY LASER SYSTEM

ApplicantSharplan Lasers, Inc., Warwick RI, US
DecisionSubstantially Equivalent, Jun 18, 1996
ReceivedApr 3, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K961279

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.