ClearanceBrief
510(k) K840919 ยท KLK Monitor, Oxygen, Cutaneous, For Infant Not Under Gas Anesthesia

DAYPAK SYS VII CATHETER CARE KIT

ApplicantCreative Care Systems, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Apr 17, 1984
ReceivedMar 1, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K840919

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.