NTI-1000— 510(k) K894097

Substantially Equivalent

Neurotek, Inc.

FDA 510(k) clearance K894097 for NTI-1000, Substantially Equivalent on 1989-09-25. Applicant: Neurotek, Inc.. Device class: 2.

Clearance details

Applicant: Neurotek, Inc.
Product code: Code QJQ
Device class: Class 2
Regulation: 21 CFR 882.5800
Advisory panel: Neurology
Date received: 1989-06-09
Decision date: 1989-09-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Olathe, KS, 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.