ClearanceBrief
510(k) K171207 ยท ODG Endoscopic Ultrasound System, Gastroenterology-Urology

FUJIFILM Ultrasonic Processor SP-900 and FUJIFILM Ultrasonic Probe PB2020-M

ApplicantFujifilm Medical Systems U.S.A, Inc., Wayne NJ, US
DecisionSubstantially Equivalent, Jan 11, 2018
ReceivedApr 25, 2017
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K171207

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.