ClearanceBrief
510(k) K931268 ยท JAA System, X-Ray, Fluoroscopic, Image-Intensified

URETERAL COMPRESSION DEVICE

ApplicantBt Medical Co., Inc., Bridgeport PA, US
DecisionSubstantially Equivalent, Jul 19, 1993
ReceivedMar 8, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K931268

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.