ClearanceBrief
510(k) K980828 ยท ETD Tube, Tympanostomy

EXMOOR MYRINGOTOMY KIT

ApplicantExmoor Plastics , Ltd., Taunton, GB
DecisionSubstantially Equivalent, Oct 22, 1998
ReceivedMar 3, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K980828

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.