ClearanceBrief
510(k) K171304 ยท MNR Ventilatory Effort Recorder

Maxxi Rip Sensor

ApplicantNeurovirtual USA, Inc., Doral FL, US
DecisionSubstantially Equivalent, Jun 24, 2019
ReceivedMay 3, 2017
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K171304

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.