ClearanceBrief
510(k) K003846 ยท LFR Glucose Dehydrogenase, Glucose

ACCU-CHEK INFORM METER

ApplicantRoche Diagnostics Corp., Indianapolis IN, US
DecisionSubstantially Equivalent, Mar 19, 2001
ReceivedDec 12, 2000
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K003846

DateFirm and productCodeLinked 510(k)
Jul 20, 2004Roche Diagnostics Corp.
ACCU-CHEK Inform meter; catalog No. 3035123.
Terminated
NBWNone listed
Jul 20, 2004Roche Diagnostics Corp.
ACCU-CHEK Inform base unit; catalog no. 3035131.
Terminated
NBWNone listed

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