Cleared Special

K172609 - CSMC Cardiac Suite

K172609 is an FDA 510(k) clearance for CSMC Cardiac Suite, manufactured by Cedars-Sinai Medical Center. The device is a Class 2 Radiology device with product code KPS cleared through the Special 510(k) pathway after a 64-day FDA review.

K172609 · Cedars-Sinai Medical Center · Radiology device
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Nov 2017
Decision
64d
Days
Class 2
Risk

K172609 is an FDA 510(k) clearance for the CSMC Cardiac Suite. Classified as System, Tomography, Computed, Emission (product code KPS), Class II - Special Controls.

Submitted by Cedars-Sinai Medical Center (Los Angeles, US). The FDA issued a Cleared decision on November 3, 2017 after a review of 64 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1200 - the FDA radiology and imaging software oversight framework. As a Special 510(k), this submission covers a manufacturer modification to an existing cleared device rather than a new device introduction.

Device pattern: Iterative device modification. Low regulatory complexity profile. This Special 510(k) clearance confirms that the manufacturer's modifications remained within the established regulatory envelope of the original cleared device.

View all Cedars-Sinai Medical Center devices

FDA 510(k) Submission Details - K172609

510(k) Number K172609 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 31, 2017
Decision Date November 03, 2017
Days to Decision 64 days
Submission Type Special
Review Panel Radiology (RA)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
43d faster than avg
Panel avg: 107d · This submission: 64d
Pathway characteristics
Modification to existing cleared device.

KPS Device Classification - Class 2, Special Controls

Product Code KPS System, Tomography, Computed, Emission
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.1200
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 - KPS System, Tomography, Computed, Emission

All 269
Devices cleared under the same product code (KPS) and FDA review panel - the closest regulatory comparables to K172609.
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