ClearanceBrief
510(k) K960907 ยท OXO Image-Intensified Fluoroscopic X-Ray System, Mobile

ORCA

ApplicantLunar Corp., Madison WI, US
DecisionSubstantially Equivalent, May 20, 1996
ReceivedMar 5, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K960907

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.