ClearanceBrief
510(k) K963706 ยท IYO System, Imaging, Pulsed Echo, Ultrasonic

PHILIPS SONO DIAGNOST 800

ApplicantHewlett-Packard Co., Andover MA, US
DecisionSubstantially Equivalent, Mar 19, 1997
ReceivedSep 16, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K963706

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.