MedHealth DVT compression Devices MHH900S/MHH900E— 510(k) K231801

Name: FDA 510(k) clearance K231801
Creator: U.S. Food and Drug Administration
Published: 2023-12-14

Substantially Equivalent

Medhealth Medical Limited

FDA 510(k) clearance K231801 for MedHealth DVT compression Devices MHH900S/MHH900E, Substantially Equivalent on 2023-12-14. Applicant: Medhealth Medical Limited. Device class: 2.

Clearance details

Applicant: Medhealth Medical Limited
Product code: Code JOW
Device class: Class 2
Regulation: 21 CFR 870.5800
Advisory panel: Cardiovascular
Date received: 2023-06-20
Decision date: 2023-12-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Shenzhen, CN

Download summary PDF View on FDA.gov ↗

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