ClearanceBrief
510(k) K883274 ยท FFG Device, Urine Flow Rate Measuring, Non-Electrical, Disposable

SURGITEK (R) UROFLOW SYSTEM

ApplicantMedical Engineering Corp., Racine WI, US
DecisionSubstantially Equivalent, Feb 8, 1989
ReceivedAug 3, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K883274

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.