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

GE TARGET SERIES 2

K Number: K896353 · Decision Dec 22, 1989
Classifications
1
FEI Numbers
7
Registration Numbers
7
Same Product Code
69
Applicant Total
169
Review Days
46

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Basic Information

Device Name
GE TARGET SERIES 2
K Number
K896353
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.5840
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
GE Medical Systems
Date Received
November 6, 1989
Decision Date
December 22, 1989
Product Code
KPQ
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
KPQ System, Simulation, Radiation Therapy

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