ClearanceBrief
510(k) K904674 ยท KRK Manometer, Blood-Pressure, Venous

CENTRAL VENOUS PRESSURE MANOMETER

ApplicantMedex, Inc., Dublin OH, US
DecisionSubstantially Equivalent, Dec 27, 1990
ReceivedOct 12, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K904674

DateFirm and productCodeLinked 510(k)
Apr 26, 2006Medex Inc
MX441B, CVP Manometer. The product is packaged in a cardboard box. The units are packed ten (10) per case. The product is labeled on the outer case with a stick-on label that reads in part, ''**mede
Terminated
KRKNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.