ClearanceBrief
510(k) K060795 ยท LRK Device, Anti-Snoring

SOMNOFIT

ApplicantStrategic Counsel Sarl, Leesburg VA, US
DecisionSubstantially Equivalent, Dec 18, 2006
ReceivedMar 23, 2006
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K060795

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.