ClearanceBrief
510(k) K202651 ยท LRK Device, Anti-Snoring

NOA Sleep Apnea and Snoring Device

ApplicantOrthoapnea S.L., Malaga, ES
DecisionSubstantially Equivalent, Feb 12, 2021
ReceivedSep 14, 2020
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K202651

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.