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Albors-Menconi Latex Corp.

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

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K891620 PATIENT EXAMINATION GLOVES (LATEX)LYY1989-05-31 View
510(k) K891621 STERILE SURGEONS' GLOVESKGO1989-04-20 View
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