ClearanceBrief
510(k) K231075 ยท IZI System, X-Ray, Angiographic

Fluorescence Accessories (YELLOW 560 and INFRARED 800 with FLOW 800 Option)

ApplicantCarl Zeiss Meditec, Inc., Dublin CA, US
DecisionSubstantially Equivalent, Jun 20, 2023
ReceivedApr 14, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K231075

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.