ClearanceBrief
510(k) K955772 ยท FMI Needle, Hypodermic, Single Lumen

CLINICARE STERILE DISPOSABLE SYRINGE/NEEDLES

ApplicantTtk Biomed, Ltd., Washington DC, US
DecisionSubstantially Equivalent, Jul 8, 1996
ReceivedDec 21, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K955772

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.