ClearanceBrief
510(k) K211817 ยท OBO Tomography, Optical Coherence

Anterion

ApplicantHeidelberg Engineering GmbH, Heidelberg, DE
DecisionSubstantially Equivalent, Nov 5, 2021
ReceivedJun 11, 2021
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K211817

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.