Utah Medical Products, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Utah Medical Products, Inc. - FDA 510(k) Cleared Devices
Recent clearances: UTAH CVX-RIPE, FINESSE 3RD GENERATION (MODELS FINESSE+ AND FINESSEII+), BT-CATH
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.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Utah Medical Products, Inc.
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
Looking for a specific device from Utah Medical Products, Inc.? Search by device name or K-number.
Search all Utah Medical Products,... devices