ClearanceBrief
510(k) K904573 ยท ODG Endoscopic Ultrasound System, Gastroenterology-Urology

PENTAX ULTRASOUND ENDOSCOPE, MODEL FG-32UA

ApplicantPentax Precision Instrument Corp., Orangeburg NY, US
DecisionSubstantially Equivalent, Jun 12, 1991
ReceivedOct 9, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K904573

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.