ClearanceBrief
510(k) K781260 ยท ETD Tube, Tympanostomy

VENTILATION TUBE SILICONE PAPARELLA TYPE

ApplicantXomed, Inc., Arnold MO, US
DecisionSubstantially Equivalent, Aug 14, 1978
ReceivedJul 24, 1978
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K781260

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.