Cleared Traditional

K923106 - SCAN BAND

K923106 is the FDA 510(k) clearance for SCAN BAND by Cook, Inc.. It is a Class 2 Radiology device (product code JAK) cleared through the Traditional 510(k) pathway after a 78-day FDA review.

K923106 · Cook, Inc. · Radiology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Sep 1992
Decision
78d
Days
Class 2
Risk

K923106 is an FDA 510(k) clearance for the SCAN BAND. Classified as System, X-ray, Tomography, Computed (product code JAK), Class II - Special Controls.

Submitted by Cook, Inc. (Ontario L4a 7x5, CA). The FDA issued a Cleared decision on September 11, 1992 after a review of 78 days - a notably fast clearance 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: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Cook, Inc. devices

Submission Details

510(k) Number K923106 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 25, 1992
Decision Date September 11, 1992
Days to Decision 78 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
29d faster than avg
Panel avg: 107d · This submission: 78d
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 581
Devices cleared under the same product code (JAK) and FDA review panel - the closest regulatory comparables to K923106.
SCAN BAND
K923110 · Cook, Inc. · Sep 1992
ARM EXTENDER FOR CT TABLES
K923111 · Cook, Inc. · Sep 1992
HEAD RESTRAINT FOR CT TABLES
K923114 · Cook, Inc. · Sep 1992
EXCEL CT TWIN
K915738 · Elscint, Inc. · Jul 1992
SHIMADZU WHOLE BODY X-RAY CT SCANNER SCT-4500TF
K921432 · Shimadzu Medical Systems · May 1992
SYTEC DENTASCAN
K914305 · General Electric Co. · Feb 1992