Q21

FDA 510(k) K221959 · Neurofield, Inc.

Substantially Equivalent

510(k) numberK221959

Submission

Device name
Q21
Applicant
Neurofield, Inc.
Bishop, CA, US
Received
July 5, 2022
Decision date
August 31, 2023
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
GWQ – Full-Montage Standard Electroencephalograph
Device class
Class II (moderate risk)
Regulation
21 CFR 882.1400
Specialty
Neurology

Acquire, display, store, and archive electroencephalographic signals from the brain using a full montage array (i.e., 16 or more electrodes) and user-specified locations

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K223644Neuronaute with IceCap 2 & IceCap 2 SmallGWQ · Special Bioserenity01/12/2023SE
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Questions and answers

When was Q21 cleared by the FDA?

Q21 (K221959) received a 510(k) decision of Substantially Equivalent on August 31, 2023, 422 days after the submission was received.

What is the product code of K221959?

The FDA product code is GWQ – Full-Montage Standard Electroencephalograph, a Class II (moderate risk) device regulated under 21 CFR 882.1400.