B&J DVT Compression Devices MHH800/MHH800SQ— 510(k) K200154

Name: FDA 510(k) clearance K200154
Creator: U.S. Food and Drug Administration
Published: 2020-07-08

Substantially Equivalent

B&J Manufacturing , Ltd.

FDA 510(k) clearance K200154 for B&J DVT Compression Devices MHH800/MHH800SQ, Substantially Equivalent on 2020-07-08. 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: 2020-01-22
Decision date: 2020-07-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Shenzhen, CN

Download summary PDF View on FDA.gov ↗

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