ClearanceBrief
510(k) K003905 ยท GWM Device, Monitoring, Intracranial Pressure

ACTI-ICP MONITORING SYSTEM

ApplicantInnerspace, Inc., Santa Ana CA, US
DecisionSubstantially Equivalent, Jun 15, 2001
ReceivedDec 19, 2000
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K003905

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.