ClearanceBrief
510(k) K983750 ยท FMI Needle, Hypodermic, Single Lumen

DEROYAL INDUSTRIES, INC TRACECART SHARPS COLLECTION CONTAINER

ApplicantDeroyal Industries, Inc., Powell TN, US
DecisionSubstantially Equivalent, Nov 30, 1998
ReceivedOct 23, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K983750

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.