NICOLET BRAINLAB SYSTEM— 510(k) K882599

Name: FDA 510(k) clearance K882599
Creator: U.S. Food and Drug Administration
Published: 1988-10-19

Substantially Equivalent

Nicolet Instrument Corp.

FDA 510(k) clearance K882599 for NICOLET BRAINLAB SYSTEM, Substantially Equivalent on 1988-10-19. Applicant: Nicolet Instrument Corp.. Device class: 2.

Clearance details

Applicant: Nicolet Instrument Corp.
Product code: Code GWK
Device class: Class 2
Regulation: 21 CFR 882.1845
Advisory panel: Neurology
Date received: 1988-06-24
Decision date: 1988-10-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Madison, WI, US

Download summary PDF View on FDA.gov ↗

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