ClearanceBrief
510(k) K060064 ยท JAF Monitor, Ultrasonic, Nonfetal

STETHOFLUX

ApplicantOdvi, Orsay, FR
DecisionSubstantially Equivalent, Apr 10, 2006
ReceivedJan 9, 2006
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K060064

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.