ClearanceBrief
510(k) K936261 ยท FMI Needle, Hypodermic, Single Lumen

CATHETER INSERTION TRAY

ApplicantMedcare Custom Packaging, Inc., E Swanzey NH, US
DecisionUnknown, Mar 10, 1994
ReceivedDec 20, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K936261

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.