ClearanceBrief
510(k) K834392 ยท DZD Tube, Orthodontic

LABIAL CUSPID TUBE

ApplicantAlexotek Co., Mchenry IL, US
DecisionSubstantially Equivalent, Feb 28, 1984
ReceivedDec 14, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K834392

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.