ClearanceBrief
510(k) K121950 ยท HAW Neurological Stereotaxic Instrument

MICROTARGETING XL STAR DRIVE SYSTEM

ApplicantFHC, Inc., Bowdoin ME, US
DecisionSubstantially Equivalent, Jul 26, 2012
ReceivedJul 3, 2012
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K121950

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.