ClearanceBrief
510(k) K833522 ยท GXW Echoencephalograph

NEURO SECTOR FIXATION DEVICE

ApplicantAdvanced Technology Laboratories, Inc., Walker MI, US
DecisionSubstantially Equivalent, May 25, 1984
ReceivedSep 19, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K833522

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.