ClearanceBrief
510(k) K914735 ยท GWM Device, Monitoring, Intracranial Pressure

VENTRICULAR PRESSURE MONITORING KIT, MODEL 110-4HM

ApplicantCamino Laboratories, Inc., San Diego CA, US
DecisionSubstantially Equivalent, Jan 17, 1992
ReceivedOct 21, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K914735

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.