NICOLET EXPERT SLEEP/WAKE ANALYSIS SYSTEM— 510(k) K873535

Name: FDA 510(k) clearance K873535
Creator: U.S. Food and Drug Administration
Published: 1987-10-26

Substantially Equivalent

Nicolet Biomedical Instruments

FDA 510(k) clearance K873535 for NICOLET EXPERT SLEEP/WAKE ANALYSIS SYSTEM, Substantially Equivalent on 1987-10-26. Applicant: Nicolet Biomedical Instruments. Device class: 2.

Clearance details

Applicant: Nicolet Biomedical Instruments
Product code: Code GWQ
Device class: Class 2
Regulation: 21 CFR 882.1400
Advisory panel: Neurology
Date received: 1987-09-01
Decision date: 1987-10-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Madison, WI, US

Download summary PDF View on FDA.gov ↗

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