ClearanceBrief
510(k) K214004 ยท FMI Needle, Hypodermic, Single Lumen

CCBIO ASCPO Needle

ApplicantCc Biotechnology Corporation, Tainan, TW
DecisionSubstantially Equivalent, Dec 13, 2022
ReceivedDec 21, 2021
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K214004

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.