Hollister, Inc. - FDA 510(k) Cleared Devices
85
Total
78
Cleared
0
Denied
Hollister, Inc. has 78 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 78 cleared submissions from 1977 to 2013. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Hollister, Inc. Filter by specialty or product code using the sidebar.
85 devices
Cleared
Apr 17, 2013
INSTAFLO BOWEL CATHETER SYSTEM KIT
Gastroenterology & Urology
128d
Cleared
Apr 22, 2010
INSTAFLO BOWEL CATHETER SYSTEM KIT
Gastroenterology & Urology
83d
Cleared
Aug 20, 2009
VAPRO INTERMITTENT CATHETER, MODEL 72062, 72082,72102, 72122, 72142, 72064,...
Gastroenterology & Urology
136d
Cleared
Feb 04, 2009
ACTIFLO INDWELLING BOWEL CATHETER SYSTEM KIT, MODELS: 32004, 32005, 32006, 32007
Gastroenterology & Urology
103d
Cleared
Apr 12, 2005
EVADRI BLADDER CONTROL SYSTEMS
Gastroenterology & Urology
47d
Cleared
May 17, 2004
RESTORE WOUND CLEANSER
General & Plastic Surgery
52d
Cleared
Mar 19, 2002
INCARE PELVIC FLOOR THERAPY SYSTEM
Gastroenterology & Urology
134d
Cleared
Mar 05, 2002
INCARE PRESSURE BIOFEEDBACK VAGINAL PRESSURE PROBE AND ANAL PRESSURE PROBE
Gastroenterology & Urology
119d
Cleared
Jan 14, 2002
INCARE ADVANCE
Gastroenterology & Urology
87d
Cleared
Jan 07, 2002
INCARE INTERMITTENT CATHETER
Gastroenterology & Urology
90d
Cleared
Dec 19, 2001
MICROGYN PLUS STIMULATION DEVICE
Gastroenterology & Urology
90d
Cleared
Aug 15, 2001
AMEDA HYGIENIKIT
Obstetrics & Gynecology
90d
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