ClearanceBrief
510(k) K130580 ยท MVL Cord, Retraction

RETRACTION PASTE

ApplicantDmg USA, Inc., Ayer MA, US
DecisionSubstantially Equivalent, Feb 25, 2014
ReceivedMar 5, 2013
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K130580

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.