NICOLET NEUROPORT/ACE SYSTEM— 510(k) K883781

Name: FDA 510(k) clearance K883781
Creator: U.S. Food and Drug Administration
Published: 1989-06-05

Substantially Equivalent

Nicolet Instrument Corp.

FDA 510(k) clearance K883781 for NICOLET NEUROPORT/ACE SYSTEM, Substantially Equivalent on 1989-06-05. Applicant: Nicolet Instrument Corp.. Device class: 2.

Clearance details

Applicant: Nicolet Instrument Corp.
Product code: Code IKN
Device class: Class 2
Regulation: 21 CFR 890.1375
Advisory panel: Physical Medicine
Date received: 1988-09-06
Decision date: 1989-06-05
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.