STIMULATOR, NIC-106 VISUAL— 510(k) K790570

Name: FDA 510(k) clearance K790570
Creator: U.S. Food and Drug Administration
Published: 1979-05-23

Substantially Equivalent

Nicolet Biomedical Instruments

FDA 510(k) clearance K790570 for STIMULATOR, NIC-106 VISUAL, Substantially Equivalent on 1979-05-23. Applicant: Nicolet Biomedical Instruments. Device class: 2.

Clearance details

Applicant: Nicolet Biomedical Instruments
Product code: Code GWE
Device class: Class 2
Regulation: 21 CFR 882.1890
Advisory panel: Neurology
Date received: 1979-03-23
Decision date: 1979-05-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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