ClearanceBrief
510(k) K946289 ยท FMI Needle, Hypodermic, Single Lumen

DEVONS POINT LOK NEEDLE PROTECTION DEVICE

ApplicantDevon Industries, Inc., Chatsworth CA, US
DecisionSubstantially Equivalent, Jul 10, 1995
ReceivedDec 27, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K946289

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.