ClearanceBrief
510(k) K001308 ยท DQA Oximeter

MODIFICATION TO ZYMED TELEMETRY SYSTEM, MODEL EASIVIEW

ApplicantAgilent Technologies, Oxnard CA, US
DecisionSubstantially Equivalent, May 17, 2000
ReceivedApr 25, 2000
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K001308

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.