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

COOPERSURGICAL MODEL 6080 SMOKE EVACUATOR SYSTEM

K Number: K910377 · Decision Apr 19, 1991
Classifications
1
FEI Numbers
193
Registration Numbers
193
Same Product Code
86
Applicant Total
41
Review Days
80

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Basic Information

Device Name
COOPERSURGICAL MODEL 6080 SMOKE EVACUATOR SYSTEM
K Number
K910377
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6740
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
CooperSurgical, Inc.
Date Received
January 29, 1991
Decision Date
April 19, 1991
Product Code
GCX
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GCX Apparatus, Suction, Operating-Room, Wall Vacuum Powered

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