Cleared Traditional

K052587 - 3D ACCU-I-TOMO XYZ SLICE VIEW TOMOGRAPH, MODEL MCT-1 EXF (FDA 510(k) Clearance)

Dec 2005
Decision
98d
Days
Class 2
Risk

K052587 is an FDA 510(k) clearance for the 3D ACCU-I-TOMO XYZ SLICE VIEW TOMOGRAPH, MODEL MCT-1 EXF. This device is classified as a System, X-ray, Tomography, Computed (Class II - Special Controls, product code JAK).

Submitted by J. Morita USA, Inc. (Washington, US). The FDA issued a Cleared decision on December 27, 2005, 98 days after receiving the submission on September 20, 2005.

This device falls under the Radiology FDA review panel. Regulated under 21 CFR 892.1750.

Submission Details

510(k) Number K052587 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 20, 2005
Decision Date December 27, 2005
Days to Decision 98 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Summary PDF

Device Classification

Product Code JAK — System, X-ray, Tomography, Computed
Device Class Class II - Special Controls
CFR Regulation 21 CFR 892.1750

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