ClearanceBrief
510(k) K810706 ยท ETD Tube, Tympanostomy

EXMOOR AURAL GROMMET AG/T5

ApplicantExmoor Plastics , Ltd., Walker MI, US
DecisionSubstantially Equivalent, Apr 14, 1981
ReceivedMar 16, 1981
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K810706

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.