ClearanceBrief
510(k) K180173 ยท HCC Device, Biofeedback

Freespira

ApplicantPalo Alto Health Sciences, Inc., Kirkland WA, US
DecisionSubstantially Equivalent, Aug 23, 2018
ReceivedJan 22, 2018
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K180173

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.