ECG CT Gating Device

FDA 510(k) K160350 · Neocoil, LLC

Substantially Equivalent

510(k) numberK160350

Submission

Device name
ECG CT Gating Device
Applicant
Neocoil, LLC
Pewaukee, WI, US
Received
February 8, 2016
Decision date
June 16, 2016
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
JAK – System, X-Ray, Tomography, Computed
Device class
Class II (moderate risk)
Regulation
21 CFR 892.1750
Specialty
Radiology

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Questions and answers

When was ECG CT Gating Device cleared by the FDA?

ECG CT Gating Device (K160350) received a 510(k) decision of Substantially Equivalent on June 16, 2016, 129 days after the submission was received.

What is the product code of K160350?

The FDA product code is JAK – System, X-Ray, Tomography, Computed, a Class II (moderate risk) device regulated under 21 CFR 892.1750.