NEUROTENS— 510(k) K896620

Substantially Equivalent

Henley Intl.

FDA 510(k) clearance K896620 for NEUROTENS, Substantially Equivalent on 1990-04-26. Applicant: Henley Intl.. Device class: 2.

Clearance details

Applicant: Henley Intl.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1989-11-21
Decision date: 1990-04-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sugar Land, TX, 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.