ClearanceBrief
510(k) K043564 ยท DQK Computer, Diagnostic, Programmable

HORIZON ANGIO CATHLAB

ApplicantMennen Medical , Ltd., Yavne, Rehovot, IL
DecisionSubstantially Equivalent, Jan 27, 2005
ReceivedDec 27, 2004
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K043564

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.