ClearanceBrief
510(k) K903729 ยท DRY Monitor, Blood-Gas, On-Line, Cardiopulmonary Bypass

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ApplicantLead-Lok, Inc., Sandpoint ID, US
DecisionSubstantially Equivalent, Sep 14, 1990
ReceivedAug 16, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K903729

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.