MERITS E700 PORCE LIFT— 510(k) K073513

Name: FDA 510(k) clearance K073513
Creator: U.S. Food and Drug Administration
Published: 2008-01-14

Substantially Equivalent

Merits Health Products Co., Ltd.

FDA 510(k) clearance K073513 for MERITS E700 PORCE LIFT, Substantially Equivalent on 2008-01-14. Applicant: Merits Health Products Co., Ltd.. Device class: 2.

Clearance details

Applicant: Merits Health Products Co., Ltd.
Product code: Code ING
Device class: Class 2
Regulation: 21 CFR 890.3930
Advisory panel: Physical Medicine
Date received: 2007-12-14
Decision date: 2008-01-14
Decision: Substantially Equivalent
Clearance type: Abbreviated
Location: Taichung, TW

Download summary PDF View on FDA.gov ↗

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Adverse events under product code ING

product code ING

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.