ClearanceBrief
510(k) K973914 ยท LXM Manipulator, Plunger-Like Joint

SENSE TECHNOLOGY INC. FRAS, SENSE TECHNOLOGY INC. PULSTAR

ApplicantSense Technology, Inc., Pittsburgh PA, US
DecisionSubstantially Equivalent, Jun 30, 1998
ReceivedOct 14, 1997
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K973914

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.