ClearanceBrief
510(k) K220518 ยท KPR System, X-Ray, Stationary

SKANRAD 400

ApplicantSkanray Technologies Limited, Mysore, IN
DecisionSubstantially Equivalent, Apr 1, 2022
ReceivedFeb 23, 2022
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K220518

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.