ClearanceBrief
510(k) K920664 ยท FFX System, Gastrointestinal Motility (Electrical)

DIAGNOSTIC ULTRASOUND/URO-GYN UPS 2020, GI VERSION

ApplicantDiagnostic Ultrasound Corp., Kirkland WA, US
DecisionSubstantially Equivalent, Dec 23, 1993
ReceivedFeb 13, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K920664

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.