FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

UTAH CVX-RIPE

K Number: K143424 · Decision Aug 28, 2015
Classifications
1
FEI Numbers
2
Registration Numbers
2
Same Product Code
1
Applicant Total
38
Review Days
270

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Basic Information

Device Name
UTAH CVX-RIPE
K Number
K143424
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.4260
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Utah Medical Products, Inc.
Date Received
December 1, 2014
Decision Date
August 28, 2015
Product Code
PFJ
Advisory Committee
Obstetrics/Gynecology
Review Advisory Committee
OB
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
PFJ Catheter, Balloon, Dilation Of Cervical Canal Prior To Labor

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K000974 FOWLER ENDOCURETTE, MODEL CUR-XXX
K965245 TBD
K970077 LIBERTY PLUS SYSTEM(PFS-300)/VAGINAL PROBE, LIBERTY PLUS(PFS-044)
K955663 ABC IN-LINE BLOOD SAMPLING KIT
K964526 LIBERTY RECTAL PELVIC FLOOR EXERCISER
K961424 INTRAN 500
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