ClearanceBrief
510(k) K955822 ยท LRK Device, Anti-Snoring

REMOVABLE HERBST APPLIANCE

ApplicantUniv. Dental Assoc. Department of Orthodontics, Buffalo NY, US
DecisionSubstantially Equivalent, Mar 20, 1996
ReceivedDec 26, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K955822

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.