ClearanceBrief
510(k) K831241 ยท HET Laparoscope, Gynecologic (And Accessories)

LASER LAPARAXOPE

ApplicantEder Instrument Co, Inc., Walker MI, US
DecisionSubstantially Equivalent, Jun 10, 1983
ReceivedApr 15, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K831241

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.