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Millimax Corp.

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

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K892922 LATEX SURGICAL GLOVESKGO1989-11-21 View
510(k) K892921 PATIENT EXAMINATION GLOVESLYY1989-09-21 View
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