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FDA 510(k)

B&J DVT Calf/Thigh Garments, Models 801/830 Series

K-Number: K201532 · 2020-09-19

ApplicantB&J Manufacturing , Ltd.
Decision Date2020-09-19
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

B&J DVT Calf/Thigh Garments, Models 801/830 Series is a medical device manufactured by B&J Manufacturing , Ltd.. It received FDA 510(k) clearance on 2020-09-19 under approval number K201532. 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 Calf/Thigh Garments, Models 801/830 Series?

B&J DVT Calf/Thigh Garments, Models 801/830 Series is a medical device that received FDA 510(k) clearance on 2020-09-19. It is manufactured by B&J Manufacturing , Ltd.. The 510(k) number is K201532.

When was B&J DVT Calf/Thigh Garments, Models 801/830 Series approved by the FDA?

B&J DVT Calf/Thigh Garments, Models 801/830 Series received FDA 510(k) clearance on 2020-09-19, under approval number K201532.

What company makes B&J DVT Calf/Thigh Garments, Models 801/830 Series?

B&J DVT Calf/Thigh Garments, Models 801/830 Series is manufactured by B&J Manufacturing , Ltd..

What is the FDA product code for B&J DVT Calf/Thigh Garments, Models 801/830 Series?

The FDA product code for B&J DVT Calf/Thigh Garments, Models 801/830 Series is JOW.

Related Clinical Trials

NCT02875964 Definition of Links Between Non-invasives Methods and Intracerebral EEG With Simultaneous Recordings. COMPLETED

Other Devices by B&J Manufacturing , Ltd.

K201547B&J DVT Foot Garments, Models 820 Series K200568B&J MHP800 Deep Vein Thrombosis (DVT) Prevention System K200154B&J DVT Compression Devices MHH800/MHH800SQ

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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