ClearanceBrief
510(k) K101331 ยท DQK Computer, Diagnostic, Programmable

LABSYSTEM PRO EP RECORDING SYSTEM V3.1 SOFTWARE

ApplicantC.R. Bard Inc., Bard Electrophysiology Division, Lowell MA, US
DecisionSubstantially Equivalent, Oct 8, 2010
ReceivedMay 11, 2010
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K101331

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.