FDA 510(k) Applications Submitted by SUE KIM

FDA 510(k) Number Submission Date Device Name Applicant
K972658 07/15/1997 MAGI ACUPUNCTURE NEEDLES DONG BANG, U.S.A.
K972659 07/15/1997 DONG BANG ACUPUNCTURE NEEDLES DONG BANG, U.S.A.


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