Utah Medical Products, Inc. - FDA 510(k) Cleared Devices
38
Total
38
Cleared
0
Denied
Utah Medical Products, Inc. has 38 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 38 cleared submissions from 1979 to 2015. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Utah Medical Products, Inc. Filter by specialty or product code using the sidebar.
38 devices
Cleared
Aug 28, 2015
UTAH CVX-RIPE
Obstetrics & Gynecology
270d
Cleared
Jan 23, 2013
FINESSE 3RD GENERATION (MODELS FINESSE+ AND FINESSEII+)
General & Plastic Surgery
90d
Cleared
Jan 11, 2011
BT-CATH
Obstetrics & Gynecology
222d
Cleared
May 23, 2007
SALINE/ CONTRAST MEDIA INFUSION CATHETER
Obstetrics & Gynecology
171d
Cleared
Sep 25, 2000
PERIPHERALLY INSERTED CENTRAL CATHETER
General Hospital
97d
Cleared
May 23, 2000
FOWLER ENDOCURETTE, MODEL CUR-XXX
Obstetrics & Gynecology
57d
Cleared
Jul 03, 1997
TBD
Obstetrics & Gynecology
184d
Cleared
May 23, 1997
LIBERTY PLUS SYSTEM(PFS-300)/VAGINAL PROBE, LIBERTY PLUS(PFS-044)
Gastroenterology & Urology
134d
Cleared
Mar 17, 1997
ABC IN-LINE BLOOD SAMPLING KIT
Anesthesiology
460d
Cleared
Feb 10, 1997
LIBERTY RECTAL PELVIC FLOOR EXERCISER
Gastroenterology & Urology
90d
Cleared
Jul 10, 1996
INTRAN 500
Obstetrics & Gynecology
89d
Cleared
Jun 27, 1996
LIBERTY LITE PFS SYSTEM
Gastroenterology & Urology
147d
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