ClearanceBrief
510(k) K945273 ยท FMI Needle, Hypodermic, Single Lumen

PRO-TECH DISPOSABLE SHARPS CONTAINERS VNC2

ApplicantPro-Tec Containers, Inc., Lake Mary FL, US
DecisionSubstantially Equivalent, Dec 14, 1994
ReceivedOct 28, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K945273

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.