FATIGMETER— 510(k) K883914

Substantially Equivalent

K. Jimbo Co., Inc.

FDA 510(k) clearance K883914 for FATIGMETER, Substantially Equivalent on 1989-10-31. Applicant: K. Jimbo Co., Inc.. Device class: 2.

Clearance details

Applicant: K. Jimbo Co., Inc.
Product code: Code GWE
Device class: Class 2
Regulation: 21 CFR 882.1890
Advisory panel: Neurology
Date received: 1988-09-16
Decision date: 1989-10-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Los Angeles, CA, 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.