FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇦 Canada

WRIST RESTRAINT FOR GE9800 C.T. TABLES

K Number: K923108 · Decision Sep 23, 1992
Classifications
1
FEI Numbers
164
Registration Numbers
164
Same Product Code
795
Applicant Total
190
Review Days
90

Basic Information

Device Name
WRIST RESTRAINT FOR GE9800 C.T. TABLES
K Number
K923108
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1750
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
COOK, INC.
Date Received
June 25, 1992
Decision Date
September 23, 1992
Product Code
JAK
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

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

Product Code Device Name
JAK System, X-Ray, Tomography, Computed

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