ClearanceBrief
510(k) K221772 ยท GYD Transducer, Tremor

NeuroRPM

ApplicantNew Touch Digital, Inc., Washington DC, US
DecisionSubstantially Equivalent, Mar 17, 2023
ReceivedJun 21, 2022
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K221772

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.