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FDA 510(k)

B&J DVT Compression Devices MHH800/MHH800SQ

K-Number: K200154 · 2020-07-08

ApplicantB&J Manufacturing , Ltd.
Decision Date2020-07-08
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

B&J DVT Compression Devices MHH800/MHH800SQ is a medical device manufactured by B&J Manufacturing , Ltd.. It received FDA 510(k) clearance on 2020-07-08 under approval number K200154. The device is classified under product code JOW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the B&J DVT Compression Devices MHH800/MHH800SQ?

B&J DVT Compression Devices MHH800/MHH800SQ is a medical device that received FDA 510(k) clearance on 2020-07-08. It is manufactured by B&J Manufacturing , Ltd.. The 510(k) number is K200154.

When was B&J DVT Compression Devices MHH800/MHH800SQ approved by the FDA?

B&J DVT Compression Devices MHH800/MHH800SQ received FDA 510(k) clearance on 2020-07-08, under approval number K200154.

What company makes B&J DVT Compression Devices MHH800/MHH800SQ?

B&J DVT Compression Devices MHH800/MHH800SQ is manufactured by B&J Manufacturing , Ltd..

What is the FDA product code for B&J DVT Compression Devices MHH800/MHH800SQ?

The FDA product code for B&J DVT Compression Devices MHH800/MHH800SQ is JOW.

Related Clinical Trials

NCT07603531 Assessment of the Efficacy of the Dynamic Decongestive System in the Maintenance Phase of Lower Limb Lymphedema NOT_YET_RECRUITING NCT05477719 Effect of Compression Stockings on the Number of Apneas/Hypopneas Per Hour of Sleep in Patients With Syndrome Obstructive Sleep Apnea/Hypopnea as Compared to no Treatment COMPLETED NCT07019662 Comparing a Suture-based System for the Removal of Arterial and Veinous ECMO Cannulas to the Standard Approach RECRUITING

Other Devices by B&J Manufacturing , Ltd.

K201532B&J DVT Calf/Thigh Garments, Models 801/830 Series K201547B&J DVT Foot Garments, Models 820 Series K200568B&J MHP800 Deep Vein Thrombosis (DVT) Prevention System

Related Devices (Code: JOW)

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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