ClearanceBrief
510(k) K925434 ยท ITX Transducer, Ultrasonic, Diagnostic

SECTOR & TRANSVAGINAL MODEL #'S SW4/5B/A,EW5/7K/A

ApplicantKretz Technik, Washington, D.C. DC, US
DecisionSubstantially Equivalent, Sep 30, 1993
ReceivedOct 28, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K925434

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.