ClearanceBrief
510(k) K023836 ยท LRK Device, Anti-Snoring

THE SUAD DEVICE

ApplicantStrong Dental, Inc., Sterling VA, US
DecisionSubstantially Equivalent, Jul 8, 2003
ReceivedNov 18, 2002
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K023836

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.