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Tillotson Corp.

FDA 510(k) & PMA Approved Devices — 4 products

Total Devices4
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K891940 PATIENT EXAM GLOVES (MFG. MOSS POINT GLOVE CO.)LYY1989-07-14 View
510(k) K893901 LATEX EXAMINATION GLOVESLYY1989-07-14 View
510(k) K891939 NON STERILE EXAM GLOVES ( TILLOTSON RUBBER CO.)LYY1989-07-14 View
510(k) K893018 HPI NON STERILE EXAM GLOVESLYY1989-06-22 View
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