ClearanceBrief
510(k) K823921 ยท LDG Kit, Earmold, Impression

PHYSICIANS CHOICE SILICONE EAR PUTTY

ApplicantSanta Barbara Medco, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Mar 28, 1983
ReceivedDec 28, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K823921

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.