NICOLET BEAM II SYSTEM— 510(k) K894629

Name: FDA 510(k) clearance K894629
Creator: U.S. Food and Drug Administration
Published: 1990-03-09

Substantially Equivalent

Nicolet Instrument Corp.

FDA 510(k) clearance K894629 for NICOLET BEAM II SYSTEM, Substantially Equivalent on 1990-03-09. Applicant: Nicolet Instrument Corp.. Device class: 1.

Clearance details

Applicant: Nicolet Instrument Corp.
Product code: Code GWS
Device class: Class 1
Regulation: 21 CFR 882.1420
Advisory panel: Neurology
Date received: 1989-07-24
Decision date: 1990-03-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Madison, WI, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.