B&J MHP800 Deep Vein Thrombosis (DVT) Prevention System— 510(k) K200568

Name: FDA 510(k) clearance K200568
Creator: U.S. Food and Drug Administration
Published: 2020-07-10

Substantially Equivalent

B&J Manufacturing , Ltd.

FDA 510(k) clearance K200568 for B&J MHP800 Deep Vein Thrombosis (DVT) Prevention System, Substantially Equivalent on 2020-07-10. Applicant: B&J Manufacturing , Ltd.. Device class: 2.

Clearance details

Applicant: B&J Manufacturing , Ltd.
Product code: Code JOW
Device class: Class 2
Regulation: 21 CFR 870.5800
Advisory panel: Cardiovascular
Date received: 2020-03-04
Decision date: 2020-07-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Shenzhen, CN

Download summary PDF View on FDA.gov ↗

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