ClearanceBrief
510(k) K844030 ยท FFG Device, Urine Flow Rate Measuring, Non-Electrical, Disposable

ACCUMETER ELECTRONIC URINEMETER SYSTEM

ApplicantTravenol Laboratories, S.A., Deerfield IL, US
DecisionSubstantially Equivalent, Nov 20, 1984
ReceivedOct 15, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K844030

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.