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

CORDGUARD II

K Number: K954619 · Decision Dec 21, 1995
Classifications
1
FEI Numbers
28
Registration Numbers
28
Same Product Code
57
Applicant Total
38
Review Days
77

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Basic Information

Device Name
CORDGUARD II
K Number
K954619
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.4530
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Utah Medical Products, Inc.
Date Received
October 5, 1995
Decision Date
December 21, 1995
Product Code
KNA
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
KNA Instrument, Manual, Specialized Obstetric-Gynecologic

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K063611 SALINE/ CONTRAST MEDIA INFUSION CATHETER
K001874 PERIPHERALLY INSERTED CENTRAL CATHETER
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
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