510(k) K201819

Device
Cadwell Apollo System
Applicant
Cadwell Industries, Inc.
510(k) number
K201819
Product code
GWQ
Decision
Substantially Equivalent (SESE)
Decision date
2020-09-29
Date received
2020-07-01
Regulation
882.1400
Classification name
Full-Montage Standard Electroencephalograph
Medical specialty
Neurology
Review panel
Neurology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Related Records

Applicant Contact

Contact
Brad Weeks
Address
909 N Kellogg St. Kennewick WA US 99336 99336

FDA Registration Numbers

Source Documents

510(k) summary PDF

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