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Makintech Corp.

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

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K893176 LATEX EXAMINATION GLOVESLYY1989-07-14 View
510(k) K883556 LATEX SURGICAL GLOVE (NON STERILE)KGO1989-02-03 View
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