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
FDA 510(k) Regulatory Record - Utah Medical Products, Inc. Obstetrics & Gynecology ✕
16 devices
Cleared
Aug 28, 2015
UTAH CVX-RIPE
Obstetrics & Gynecology
270d
Cleared
Jan 11, 2011
BT-CATH
Obstetrics & Gynecology
222d
Cleared
May 23, 2007
SALINE/ CONTRAST MEDIA INFUSION CATHETER
Obstetrics & Gynecology
171d
Cleared
May 23, 2000
FOWLER ENDOCURETTE, MODEL CUR-XXX
Obstetrics & Gynecology
57d
Cleared
Jul 03, 1997
TBD
Obstetrics & Gynecology
184d
Cleared
Jul 10, 1996
INTRAN 500
Obstetrics & Gynecology
89d
Cleared
Apr 29, 1996
ASPIRATION/COAGULATION ELECTRODE ACE-311 & ACE-511
Obstetrics & Gynecology
174d
Cleared
Feb 20, 1996
INTRAN PLUS
Obstetrics & Gynecology
84d
Cleared
Dec 21, 1995
CORDGUARD II
Obstetrics & Gynecology
77d
Cleared
Apr 11, 1995
LUMIN
Obstetrics & Gynecology
267d
Cleared
Dec 12, 1994
FINESSE IEC/601
Obstetrics & Gynecology
272d
Cleared
May 26, 1993
BUBBLE TOCO
Obstetrics & Gynecology
499d
Cleared
Sep 18, 1991
UTAH ESSU
Obstetrics & Gynecology
299d
Cleared
Jun 19, 1991
INTRAN PLUS
Obstetrics & Gynecology
189d
Cleared
Mar 29, 1991
COMBO FETAL SCALP ELECTRODE/LEGPLATE
Obstetrics & Gynecology
88d
Cleared
Feb 26, 1987
IUC - INTRAUTERINE CATHETER
Obstetrics & Gynecology
211d