ClearanceBrief
510(k) K060708 ยท MNR Ventilatory Effort Recorder

SOMNOSCREEN

ApplicantSomnomedics GmbH & Co. KG, Washington DC, US
DecisionSubstantially Equivalent, Jan 24, 2007
ReceivedMar 16, 2006
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K060708

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.