ClearanceBrief
510(k) K111392 ยท MQX Needle, Acupuncture, Single Use

WOOJEON ACUPUNCTURE NEEDLE (=SERA ACUPUNCTURE NEEDLE)

ApplicantWoojeon Company, Pittsburgh PA, US
DecisionSubstantially Equivalent, Nov 4, 2011
ReceivedMay 18, 2011
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K111392

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.