ClearanceBrief
510(k) K080983 ยท MNR Ventilatory Effort Recorder

PROVENT NASAL CANNULA

ApplicantVentus Medical, Inc., Belmont CA, US
DecisionSubstantially Equivalent, Aug 7, 2008
ReceivedApr 7, 2008
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K080983

DateFirm and productCodeLinked 510(k)
Sep 19, 2010Ventus Medical, Inc.
The Provent Nasal Cannula is a nasal appliance device placed in both nostrils intended to be used for transmission of respiratory airflow signals between the Provent Professional Sleep Apnea Therapy d
Terminated
MNRNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.