ClearanceBrief
510(k) K873721 ยท LGH Instrument, Cast Removal, Ac-Powered

PLASTER VACUUM, 115V MODEL NO. 4183-160

ApplicantMartin Medical, Desoto KS, US
DecisionSubstantially Equivalent, Dec 7, 1987
ReceivedSep 15, 1987
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K873721

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.