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FDA 510(k)

B&J MHP800 Deep Vein Thrombosis (DVT) Prevention System

K-Number: K200568 · 2020-07-10

ApplicantB&J Manufacturing , Ltd.
Decision Date2020-07-10
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

B&J MHP800 Deep Vein Thrombosis (DVT) Prevention System is the device name listed in this FDA 510(k) record. The listed applicant is B&J Manufacturing , Ltd.. It received FDA 510(k) clearance on 2020-07-10 under 510(k) number K200568. 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 MHP800 Deep Vein Thrombosis (DVT) Prevention System?

B&J MHP800 Deep Vein Thrombosis (DVT) Prevention System is a medical device that received FDA 510(k) clearance on 2020-07-10. The listed applicant is B&J Manufacturing , Ltd.. The 510(k) number is K200568.

When did B&J MHP800 Deep Vein Thrombosis (DVT) Prevention System receive FDA 510(k) clearance?

B&J MHP800 Deep Vein Thrombosis (DVT) Prevention System received FDA 510(k) clearance on 2020-07-10, under 510(k) number K200568.

Who is the listed applicant for B&J MHP800 Deep Vein Thrombosis (DVT) Prevention System?

The FDA 510(k) record lists B&J Manufacturing , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for B&J MHP800 Deep Vein Thrombosis (DVT) Prevention System?

The FDA product code for B&J MHP800 Deep Vein Thrombosis (DVT) Prevention System is JOW.

Related Clinical Trials

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Other records listing B&J Manufacturing , Ltd. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K201532B&J DVT Calf/Thigh Garments, Models 801/830 SeriesK201547B&J DVT Foot Garments, Models 820 SeriesK200154B&J DVT Compression Devices MHH800/MHH800SQ

Related Devices (Code: JOW)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K253555Flexitouch® Plus Advanced Pneumatic Compression SystemTactile MedicalK253386DVT GarmentVistar Medical Supplies Co., Ltd.K250242Compression Therapy Device (LGT-2202DVT)Guangzhou Longest Medical Technology Co., Ltd.K254267NanoPress 760A-BT (760A-BT)Mego Afek , Ltd.K250974Bio Arterial Deluxe (IC-BAP-DX)Bio Compression Systems, Inc.K250190Sequential Compression System (SCD600)Shenzhen Comen Medical Instruments Co.,Ltd

Official Source

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

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