NICOLET AMP 6R11 SYSTEM— 510(k) K871678

Name: FDA 510(k) clearance K871678
Creator: U.S. Food and Drug Administration
Published: 1987-07-16

Substantially Equivalent

Nicolet Biomedical Instruments

FDA 510(k) clearance K871678 for NICOLET AMP 6R11 SYSTEM, Substantially Equivalent on 1987-07-16. Applicant: Nicolet Biomedical Instruments. Device class: 2.

Clearance details

Applicant: Nicolet Biomedical Instruments
Product code: Code GWL
Device class: Class 2
Regulation: 21 CFR 882.1835
Advisory panel: Neurology
Date received: 1987-04-28
Decision date: 1987-07-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Madison, WI, US

Download summary PDF View on FDA.gov ↗

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