AXON II BRAND OF DUAL CHANNEL TENS— 510(k) K850860

Name: FDA 510(k) clearance K850860
Creator: U.S. Food and Drug Administration
Published: 1985-05-31

Substantially Equivalent

Cassandra Electronics Corp.

FDA 510(k) clearance K850860 for AXON II BRAND OF DUAL CHANNEL TENS, Substantially Equivalent on 1985-05-31. Applicant: Cassandra Electronics Corp.. Device class: 2.

Clearance details

Applicant: Cassandra Electronics Corp.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1985-03-01
Decision date: 1985-05-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Minneapolis, MN, US

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