ClearanceBrief
510(k) K131630 ยท LIO Device, Specimen Collection

PURITAN AMIES MEDIUM COLLECTION AND TRANSPORT SYSTEM

ApplicantPuritan Medical Products, LLC, Guilford ME, US
DecisionSubstantially Equivalent, Oct 21, 2013
ReceivedJun 4, 2013
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K131630

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.