ClearanceBrief
510(k) K121282 ยท NXV Diagnostic Light, Soft Tissue Detector

MICROLUX/DL MICROLUX/BLU BIO/SCREEN

ApplicantAddent, Inc., Danbury CT, US
DecisionSubstantially Equivalent, Jul 24, 2012
ReceivedApr 30, 2012
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K121282

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.