RELIEEV Suction Curette (Flexible 3.0/ Standard 3.6)— 510(k) K240434

Name: FDA 510(k) clearance K240434
Creator: U.S. Food and Drug Administration
Published: 2024-09-25

Substantially Equivalent

Li Medical Corporation , Ltd.

FDA 510(k) clearance K240434 for RELIEEV Suction Curette (Flexible 3.0/ Standard 3.6), Substantially Equivalent on 2024-09-25. Applicant: Li Medical Corporation , Ltd.. Device class: 2.

Clearance details

Applicant: Li Medical Corporation , Ltd.
Product code: Code HHK
Device class: Class 2
Regulation: 21 CFR 884.1175
Advisory panel: Obstetrics/Gynecology
Date received: 2024-02-14
Decision date: 2024-09-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: New Taipei City, TW

Download summary PDF View on FDA.gov ↗

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