ClearanceBrief
510(k) K863479 ยท GWM Device, Monitoring, Intracranial Pressure

MODIFIED ICT/B INTRACRANIAL PRESS. TRANS. EPIDURAL

ApplicantMedical Measurements, Inc., Hackensack NJ, US
DecisionSubstantially Equivalent, Oct 14, 1986
ReceivedSep 9, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K863479

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.