ClearanceBrief
510(k) K931282 ยท EXQ Cystometer, Electrical Recording

VOLUME TRANSDUCER

ApplicantLife-Tech Intl., Inc., Houston TX, US
DecisionSubstantially Equivalent, Sep 17, 1993
ReceivedMar 12, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K931282

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.