ClearanceBrief
510(k) K972348 ยท ITX Transducer, Ultrasonic, Diagnostic

HP ENDOVAGINAL/ENDORECTAL PROBE, HP IMAGE POINT ULTRASOUND SYSTEM

ApplicantHewlett-Packard Co., Andover MA, US
DecisionSubstantially Equivalent, Jul 24, 1997
ReceivedJun 24, 1997
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K972348

DateFirm and productCodeLinked 510(k)
Aug 22, 2025Philips Ultrasound, Inc
7.5MHZ Endo Transducer Probe
Open, Classified
ITXNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.