FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇪 Germany

COOPERSURGICAL LAPAROSCOPIC INSTRUMENTS

K Number: K021237 · Decision Apr 10, 2003
Classifications
1
FEI Numbers
153
Registration Numbers
153
Same Product Code
337
Applicant Total
41
Review Days
357

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Basic Information

Device Name
COOPERSURGICAL LAPAROSCOPIC INSTRUMENTS
K Number
K021237
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.1720
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
CooperSurgical, Inc.
Date Received
April 18, 2002
Decision Date
April 10, 2003
Product Code
HET
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
HET Laparoscope, Gynecologic (And Accessories)

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K190639 Endosee System
K182959 Wallace Dual Lumen Oocyte Recovery System
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