ClearanceBrief
510(k) K232702 ยท ETD Tube, Tympanostomy

Solo+ Tympanostomy Tube Device (TTD)

ApplicantAventamed Dac, Bishopstown, IE
DecisionSubstantially Equivalent, May 20, 2024
ReceivedSep 5, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K232702

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.