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Ansell, Inc.

FDA 510(k) & PMA Approved Devices — 30 products

Total Devices30
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K984392 ANSELL CONDOMSHIS1999-07-21 View
510(k) K983518 LIFESTYLES XTRA PLEASUREHIS1999-07-06 View
510(k) K940047 SPERMICIDALLY LUBRICATED CONDOMHIS1995-12-19 View
510(k) K953379 HYPOALLERGENIC POWDERED AMBIDEXTROUS COAGULATN DIPPED LATEX EXAMINATION GLOVELYY1995-09-27 View
510(k) K945766 HYPOALLERGENIC POWDERED AMBIDEXTROUS PATIENT EXAMINATION GLOVESLYY1995-08-07 View
510(k) K945767 POWDER FREE, HYPOALLERGENIC AMBIDEXTROUS PATIENT EXAMINATION GLOVESLYY1995-03-02 View
510(k) K940045 CONDOMHIS1995-01-30 View
510(k) K940046 NON-LUBRICATED CONDOMHIS1995-01-30 View
510(k) K913766 ANSELL NO POWDER AMBI PATIENT EXAMINATION GLOVESLYY1993-03-11 View
510(k) K914760 LATEX EXAMINATION GLOVESLYY1992-01-17 View
510(k) K903108 PATIENT EXAM GLOVES (FINISH W/USP STARCH POWDER)LYY1990-08-29 View
510(k) K903107 PATIENT EXAM GLOVES (DUSTED W/USP STARCH POWDER)LYY1990-08-29 View
510(k) K901112 G.S.A. COLORED CONDOMSHIS1990-03-27 View
510(k) K901111 NUDA (CURRENTLY CALLED ULTRA SENSITIVE)HIS1990-03-27 View
510(k) K897081 ANSELL CONFORM GREEN EXAMINATION GLOVESLYZ1990-03-26 View
510(k) K895660 ANSELL DENTA GLOVESLYY1990-01-02 View
510(k) K892289 PATIENT EXAMINATION GLOVES (LATEX)LYY1989-06-23 View
510(k) K892288 PATIENT EXAMINATION GLOVES (LATEX)LYY1989-06-09 View
510(k) K892106 STERILE EXAM GLOVESLYY1989-05-31 View
510(k) K892325 NON-STERILE EXAM GLOVESLYY1989-05-31 View
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