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

CT PROSPEED FAMILY

K Number: K944013 · Decision Feb 7, 1995
Classifications
1
FEI Numbers
164
Registration Numbers
164
Same Product Code
795
Applicant Total
166
Review Days
175

Basic Information

Device Name
CT PROSPEED FAMILY
K Number
K944013
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1750
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
GE MEDICAL SYSTEMS
Date Received
August 16, 1994
Decision Date
February 7, 1995
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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