VECTOR SEIGE 2023645 AC POWERED STIMU-— 510(k) K833305

Name: FDA 510(k) clearance K833305
Creator: U.S. Food and Drug Administration
Published: 1983-11-28

Substantially Equivalent

Metronex Engineering

FDA 510(k) clearance K833305 for VECTOR SEIGE 2023645 AC POWERED STIMU-, Substantially Equivalent on 1983-11-28. Applicant: Metronex Engineering. Device class: 2.

Clearance details

Applicant: Metronex Engineering
Product code: Code LIH
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1983-09-23
Decision date: 1983-11-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, 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.