Ansell, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ANSELL CONDOMS, LIFESTYLES XTRA PLEASURE, SPERMICIDALLY LUBRICATED CONDOM
30
Total
30
Cleared
0
Denied
FDA 510(k) Regulatory Record - Ansell, Inc. General Hospital ✕
18 devices
Cleared
Sep 27, 1995
HYPOALLERGENIC POWDERED AMBIDEXTROUS COAGULATN DIPPED LATEX EXAMINATION GLOVE
General Hospital
70d
Cleared
Aug 07, 1995
HYPOALLERGENIC POWDERED AMBIDEXTROUS PATIENT EXAMINATION GLOVES
General Hospital
259d
Cleared
Mar 02, 1995
POWDER FREE, HYPOALLERGENIC AMBIDEXTROUS PATIENT EXAMINATION GLOVES
General Hospital
101d
Cleared
Mar 11, 1993
ANSELL NO POWDER AMBI PATIENT EXAMINATION GLOVES
General Hospital
567d
Cleared
Jan 17, 1992
LATEX EXAMINATION GLOVES
General Hospital
87d
Cleared
Aug 29, 1990
PATIENT EXAM GLOVES (DUSTED W/USP STARCH POWDER)
General Hospital
51d
Cleared
Aug 29, 1990
PATIENT EXAM GLOVES (FINISH W/USP STARCH POWDER)
General Hospital
50d
Cleared
Mar 26, 1990
ANSELL CONFORM GREEN EXAMINATION GLOVES
General Hospital
97d
Cleared
Jan 02, 1990
ANSELL DENTA GLOVES
General Hospital
104d
Cleared
Jun 23, 1989
PATIENT EXAMINATION GLOVES (LATEX)
General Hospital
78d
Cleared
Jun 09, 1989
PATIENT EXAMINATION GLOVES (LATEX)
General Hospital
64d
Cleared
May 31, 1989
STERILE EXAM GLOVES
General Hospital
58d