MF-500, MODIFICATION— 510(k) K911144

Substantially Equivalent

Elcot, Inc.

FDA 510(k) clearance K911144 for MF-500, MODIFICATION, Substantially Equivalent on 1991-10-18. Applicant: Elcot, Inc.. Device class: 2.

Clearance details

Applicant: Elcot, Inc.
Product code: Code QGH
Device class: Class 2
Regulation: 21 CFR 882.5940
Advisory panel: Neurology
Date received: 1991-02-25
Decision date: 1991-10-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: New York, NY, 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.