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

3D ACCU-I-TOMO XYZ SLICE VIEW TOMOGRAPH

K Number: K030450 · Decision May 6, 2003
Classifications
1
FEI Numbers
164
Registration Numbers
164
Same Product Code
795
Applicant Total
47
Review Days
84

Basic Information

Device Name
3D ACCU-I-TOMO XYZ SLICE VIEW TOMOGRAPH
K Number
K030450
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1750
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
J. MORITA USA, INC.
Date Received
February 11, 2003
Decision Date
May 6, 2003
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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