ClearanceBrief
510(k) K862286 ยท NFQ Device, Dental Sonography, For Monitoring Jaw Sounds

ARTHROPHONOMETER

ApplicantArthrotek, Inc., West Hartford CT, US
DecisionSubstantially Equivalent, Jan 7, 1987
ReceivedJun 16, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K862286

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.