AGARRELIEF 10 TRANSCUTANEOUS ELEC NERVE STIMULATOR— 510(k) K905526

Name: FDA 510(k) clearance K905526
Creator: U.S. Food and Drug Administration
Published: 1991-06-21

Substantially Equivalent

Agar Ginosar Electronics

FDA 510(k) clearance K905526 for AGARRELIEF 10 TRANSCUTANEOUS ELEC NERVE STIMULATOR, Substantially Equivalent on 1991-06-21. Applicant: Agar Ginosar Electronics. Device class: 2.

Clearance details

Applicant: Agar Ginosar Electronics
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1990-12-10
Decision date: 1991-06-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ginosar, IL

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