ClearanceBrief
510(k) K854549 ยท FMI Needle, Hypodermic, Single Lumen

MONOJECT STERILE M400 PLASTIC&STERILE M401 ALUMINU

ApplicantSherwood Medical Co., St. Louis MO, US
DecisionSubstantially Equivalent, Feb 4, 1986
ReceivedNov 13, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K854549

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.