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

COOPERSURGICAL DIGITAL COLPOSCOPY SYSTEM

K Number: K972630 · Decision Feb 2, 1998
Classifications
1
FEI Numbers
19
Registration Numbers
19
Same Product Code
55
Applicant Total
41
Review Days
203

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Basic Information

Device Name
COOPERSURGICAL DIGITAL COLPOSCOPY SYSTEM
K Number
K972630
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.1630
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
CooperSurgical, Inc.
Date Received
July 14, 1997
Decision Date
February 2, 1998
Product Code
HEX
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
HEX Colposcope (And Colpomicroscope)

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Other Clearances by CooperSurgical, Inc.

K Number Device Name
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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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