ClearanceBrief
510(k) K870877 ยท ETD Tube, Tympanostomy

BIO-VENT REUTER BOBBIN TUBE

ApplicantRichards Medical Co., Inc., Memphis TN, US
DecisionSubstantially Equivalent, Mar 26, 1987
ReceivedMar 3, 1987
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K870877

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.