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

TARGOBEAM

K Number: K970819 · Decision Jul 14, 1997
Classifications
1
FEI Numbers
163
Registration Numbers
163
Same Product Code
818
Applicant Total
57
Review Days
131

Basic Information

Device Name
TARGOBEAM
K Number
K970819
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1750
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ferguson Medical
Date Received
March 5, 1997
Decision Date
July 14, 1997
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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