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Kerala Rubber & Reclaims, Ltd.

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

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K933602 PATIENT EXAMINATION GLOVELYY1995-01-02 View
510(k) K894452 KRR GLOVE, PATIENT EXAMINATION GLOVESLYY1989-08-09 View
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