ClearanceBrief
510(k) K042907 ยท FMI Needle, Hypodermic, Single Lumen

NEEDLE INCAPACITATOR (NEEDLE GUARD)

ApplicantPdmp, Inc., Crofton MD, US
DecisionSubstantially Equivalent, Dec 22, 2004
ReceivedOct 21, 2004
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K042907

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.