AGAR 8000 TENS— 510(k) K832851

Substantially Equivalent

Kimed Industries, Inc.

FDA 510(k) clearance K832851 for AGAR 8000 TENS, Substantially Equivalent on 1983-10-28. Applicant: Kimed Industries, Inc.. Device class: 2.

Clearance details

Applicant: Kimed Industries, Inc.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1983-08-22
Decision date: 1983-10-28
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.