TENS GB1001 DEVICE— 510(k) K850855

Substantially Equivalent

Medicon, Inc.

FDA 510(k) clearance K850855 for TENS GB1001 DEVICE, Substantially Equivalent on 1986-01-09. Applicant: Medicon, Inc.. Device class: 2.

Clearance details

Applicant: Medicon, Inc.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1985-03-01
Decision date: 1986-01-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Norwalk, CT, 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.