ClearanceBrief
510(k) K834354 ยท HOG Burr, Corneal, Battery-Powered

OPHTEC RUST RING REMOVER

ApplicantJedmed Instrument Co., Mchenry IL, US
DecisionSubstantially Equivalent, Mar 19, 1984
ReceivedDec 13, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K834354

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.