ClearanceBrief
510(k) K103455 ยท GEX Powered Laser Surgical Instrument

SPECTRA LASER SYSTEM

ApplicantLutronic Corporation, Princeton Junction NJ, US
DecisionSubstantially Equivalent, Apr 28, 2011
ReceivedNov 23, 2010
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K103455

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.