ClearanceBrief
510(k) K922984 ยท LRK Device, Anti-Snoring

ORTHODONTIC BITE

ApplicantAmerican Orthodontics, Sheboygan WI, US
DecisionSubstantially Equivalent, Mar 31, 1993
ReceivedJun 22, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K922984

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.