ClearanceBrief
510(k) K082603 ยท NXV Diagnostic Light, Soft Tissue Detector

TRIMIRA OCS 3000

ApplicantRemicalm, LLC, Houston TX, US
DecisionSubstantially Equivalent, Dec 12, 2008
ReceivedSep 8, 2008
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K082603

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.