ClearanceBrief
510(k) K022420 ยท HCG Device, Neurovascular Embolization

MICRUS STRETCH-RESISTANT MICROCOIL SYSTEM, MSR01

ApplicantMicrus Corp., Mountain View CA, US
DecisionSubstantially Equivalent, Oct 22, 2002
ReceivedJul 24, 2002
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K022420

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.