HARIKY, MODEL GK-7— 510(k) K860772

Substantially Equivalent

K-Mot, Inc.

FDA 510(k) clearance K860772 for HARIKY, MODEL GK-7, Substantially Equivalent on 1986-05-09. Applicant: K-Mot, Inc.. Device class: 2.

Clearance details

Applicant: K-Mot, Inc.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1986-03-03
Decision date: 1986-05-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Glendale, AZ, 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.