ClearanceBrief
510(k) K200756 ยท MWP Cabinet, X-Ray System

Kubtec Mozart Supra

ApplicantKub Technologies, Inc., Stratford CT, US
DecisionSubstantially Equivalent, Jun 12, 2020
ReceivedMar 24, 2020
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K200756

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.