ClearanceBrief
510(k) K833909 ยท ETD Tube, Tympanostomy

VENTRESCREEN BETA-HCG ENZYME IMMUNO

ApplicantVxr, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Nov 21, 1983
ReceivedNov 14, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K833909

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.