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Kimble-Terumo, Inc.

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

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K801015 PREZAPAK L ARTERIAL BLOOD SAMPLING KITGIM1980-05-14 View
510(k) K792587 VENOJECT AUTOSEPJKA1980-01-17 View
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