ClearanceBrief
510(k) K833910 ยท ETD Tube, Tympanostomy

TSH RIA

ApplicantSyncor Intl. Corp., Mchenry IL, US
DecisionSubstantially Equivalent, Nov 22, 1983
ReceivedNov 14, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K833910

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.