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Precident Corp.

FDA 510(k) & PMA Approved Devices — 2 products

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K913019 PDI PARALLEL SIDED POST KITELR1991-10-02 View
510(k) K911323 FLUX-N-ALLEJH1991-09-30 View
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