ClearanceBrief
510(k) K860357 ยท LNK Laser For Gastro-Urology Use

HGM, INC. LASERCATH (STERILE)

ApplicantHgm, Inc., Salt Lake City UT, US
DecisionSubstantially Equivalent, Apr 7, 1986
ReceivedJan 30, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K860357

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.