ClearanceBrief
510(k) K232237 ยท PHZ Abnormal Breath Sound Device

Tyto Insights for Wheeze Detection

ApplicantTyto Care , Ltd., Netanya, IL
DecisionSubstantially Equivalent, Dec 13, 2023
ReceivedJul 28, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K232237

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.