ClearanceBrief
510(k) K914006 ยท ITX Transducer, Ultrasonic, Diagnostic

BIPLANE TRANSRECTAL PROBE

ApplicantBiosound, Inc., Indianapolis IN, US
DecisionSubstantially Equivalent, Apr 2, 1992
ReceivedSep 9, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K914006

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.