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

3D ACCU-I-TOMO XYZ SLICE VIEW TOMOGRAPH, MODEL MCT-1F8/F17

K Number: K073695 · Decision Apr 9, 2008
Classifications
1
FEI Numbers
163
Registration Numbers
163
Same Product Code
818
Applicant Total
52
Review Days
100

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Basic Information

Device Name
3D ACCU-I-TOMO XYZ SLICE VIEW TOMOGRAPH, MODEL MCT-1F8/F17
K Number
K073695
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
December 31, 2007
Decision Date
April 9, 2008
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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