ClearanceBrief
510(k) K800728 ยท ETD Tube, Tympanostomy

PAPARELL TYPE 2, BIOLITE COATED SILI-

ApplicantXomed, Inc., Arnold MO, US
DecisionSubstantially Equivalent, Apr 16, 1980
ReceivedApr 1, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K800728

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.