MEDX 1000 SERIES— 510(k) K020017

Name: FDA 510(k) clearance K020017
Creator: U.S. Food and Drug Administration
Published: 2002-07-12

Substantially Equivalent

Medx Electronics, Inc.

FDA 510(k) clearance K020017 for MEDX 1000 SERIES, Substantially Equivalent on 2002-07-12. Applicant: Medx Electronics, Inc.. Device class: 2.

Clearance details

Applicant: Medx Electronics, Inc.
Product code: Code ILY
Device class: Class 2
Regulation: 21 CFR 890.5500
Advisory panel: Physical Medicine
Date received: 2002-01-03
Decision date: 2002-07-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Alexandria, VA, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code ILY

product code ILY

Death: 3
Total: 3

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.