ClearanceBrief
510(k) K943849 ยท ETD Tube, Tympanostomy

GROMMENT STYLE VENTURI TUBE

ApplicantMicromed Development Corp., Clearwater FL, US
DecisionSubstantially Equivalent, Sep 2, 1994
ReceivedAug 4, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K943849

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.