ClearanceBrief
510(k) K891485 ยท LMB Device, Digital Image Storage, Radiological

ANGIOTEC FMX-2220 SYSTEM

ApplicantAndros Analyzers, Inc., Berkeley CA, US
DecisionSubstantially Equivalent, May 5, 1989
ReceivedMar 17, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K891485

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.