Cleared Traditional

K935487 - SHIMADZU WHOLE BODY X-RAY CT SCANNER SC...

K935487 is the FDA 510(k) clearance for SHIMADZU WHOLE BODY X-RAY CT SCANNER SC... by Shimadzu Corp.. It is a Class 2 Radiology device (product code JAK) cleared through the Traditional 510(k) pathway after a 232-day FDA review.

K935487 · Shimadzu Corp. · Radiology device
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Jul 1994
Decision
232d
Days
Class 2
Risk

K935487 is an FDA 510(k) clearance for the SHIMADZU WHOLE BODY X-RAY CT SCANNER SCT-4800TF. Classified as System, X-ray, Tomography, Computed (product code JAK), Class II - Special Controls.

Submitted by Shimadzu Corp. (Torrance, US). The FDA issued a Cleared decision on July 5, 1994 after a review of 232 days - an extended review cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1750 - the FDA radiology and imaging software oversight framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Radiology review framework, consistent with the majority of Class II 510(k) submissions.

View all Shimadzu Corp. devices

Submission Details

510(k) Number K935487 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 15, 1993
Decision Date July 05, 1994
Days to Decision 232 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
125d slower than avg
Panel avg: 107d · This submission: 232d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code JAK System, X-ray, Tomography, Computed
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.1750
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Radiology devices follow this clearance model.

Regulatory Peers - JAK System, X-ray, Tomography, Computed

All 604
Devices cleared under the same product code (JAK) and FDA review panel - the closest regulatory comparables to K935487.
HISPEED ADVANTAGE II
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COMPUTERIZED TOMOGRAPHY X-RAY SYSTEM OPTION
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