ClearanceBrief
510(k) K113201 ยท LQZ Device, Jaw Repositioning

NARVAL CC

ApplicantResmed Sas, San Diego CA, US
DecisionSubstantially Equivalent, Dec 1, 2011
ReceivedOct 31, 2011
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K113201

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.