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

FINESSE IEC/601

K Number: K941251 · Decision Dec 12, 1994
Classifications
1
FEI Numbers
66
Registration Numbers
66
Same Product Code
52
Applicant Total
38
Review Days
272

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Basic Information

Device Name
FINESSE IEC/601
K Number
K941251
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.4120
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Utah Medical Products, Inc.
Date Received
March 15, 1994
Decision Date
December 12, 1994
Product Code
HGI
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
HGI Electrocautery, Gynecologic (And Accessories)

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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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