ClearanceBrief
510(k) K172991 ยท LRK Device, Anti-Snoring

Advanced Dental Applicance

ApplicantDasoft Partners, San Diego CA, US
DecisionSubstantially Equivalent, Jul 10, 2018
ReceivedSep 27, 2017
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K172991

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.