K-STIM CLEAR— 510(k) K922202

Substantially Equivalent

Katecho, Inc.

FDA 510(k) clearance K922202 for K-STIM CLEAR, Substantially Equivalent on 1993-05-17. Applicant: Katecho, Inc.. Device class: 2.

Clearance details

Applicant: Katecho, Inc.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1992-05-11
Decision date: 1993-05-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Des Moines, IA, 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.