ClearanceBrief
510(k) K770528 ยท FMI Needle, Hypodermic, Single Lumen

NEEDLE, MEMBRANE

ApplicantAmerican Viggo, Walker MI, US
DecisionSubstantially Equivalent, Apr 29, 1977
ReceivedMar 18, 1977
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K770528

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.