CADWELL FLEX EEG/PSG— 510(k) K133355

Substantially Equivalent

Cadwell Industries, Inc.

FDA 510(k) clearance K133355 for CADWELL FLEX EEG/PSG, Substantially Equivalent on 2014-01-29. Applicant: Cadwell Industries, Inc.. Device class: 2.

Clearance details

Applicant: Cadwell Industries, Inc.
Product code: Code GWQ
Device class: Class 2
Regulation: 21 CFR 882.1400
Advisory panel: Neurology
Date received: 2013-10-31
Decision date: 2014-01-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Kennewick, WA, US

Download summary PDF View on FDA.gov ↗

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