ClearanceBrief
510(k) K936275 ยท ETD Tube, Tympanostomy

TYMPOVENT

ApplicantAtos Medical AB, Horby, Sweden, SE
DecisionSubstantially Equivalent, May 5, 1994
ReceivedDec 30, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K936275

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.