AXION IV GOLDLINE SERIES— 510(k) K862602

Name: FDA 510(k) clearance K862602
Creator: U.S. Food and Drug Administration
Published: 1986-12-22

Substantially Equivalent

Ventura Medical Electronics

FDA 510(k) clearance K862602 for AXION IV GOLDLINE SERIES, Substantially Equivalent on 1986-12-22. Applicant: Ventura Medical Electronics. Device class: 2.

Clearance details

Applicant: Ventura Medical Electronics
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1986-07-08
Decision date: 1986-12-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Shawnee, KS, US

Download summary PDF View on FDA.gov ↗

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