ClearanceBrief
510(k) K943987 ยท GWM Device, Monitoring, Intracranial Pressure

OPX-VX FEBEROPTIC INTRACRANIAL PRESSURE MONITORING CATHETER WITH DRAINAGE

ApplicantInnerspace Medical, Inc., Irvine CA, US
DecisionSubstantially Equivalent, Dec 7, 1994
ReceivedAug 16, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K943987

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.