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Duflex Products Sdn. Bhd.

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

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K891884 PATIENT EXAMINATION GLOVES (LATEX)LYY1989-04-13 View
510(k) K891322 DISPOSABLE LATEX EXAMINATION GLOVESLYY1989-03-31 View
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