ClearanceBrief
510(k) K940648 ยท GWM Device, Monitoring, Intracranial Pressure

CORDIS DISPOSABLE ICP PRESSURE TRANSDUCER

ApplicantCordis Corp., Miami Lakes FL, US
DecisionSubstantially Equivalent, Mar 1, 1995
ReceivedFeb 15, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K940648

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.