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

LEEP SYSTEM 1000

K Number: K952483 · Decision Oct 6, 1995
Classifications
1
FEI Numbers
66
Registration Numbers
66
Same Product Code
52
Applicant Total
41
Review Days
129

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Basic Information

Device Name
LEEP SYSTEM 1000
K Number
K952483
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.4120
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
CooperSurgical, Inc.
Date Received
May 30, 1995
Decision Date
October 6, 1995
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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Other Clearances by CooperSurgical, Inc.

K Number Device Name
K243799 Fetal Pillow
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K223064 ALLY II Uterine Positioning System™ (UPS)
K201086 Advincula Delineator Uterine Manipulator
K200038 Endosee System
K191020 G210 InviCell Plus with SignipHy pH monitoring
K191291 Wallace Dual Lumen Oocyte Recovery System
K190639 Endosee System
K182959 Wallace Dual Lumen Oocyte Recovery System
K183020 Endosee System
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