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FDA 510(k)

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

K-Number: K200568 · 2020-07-10

Decision Date2020-07-10
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

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

When was B&J MHP800 Deep Vein Thrombosis (DVT) Prevention System approved by the FDA?

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

What company makes B&J MHP800 Deep Vein Thrombosis (DVT) Prevention System?

B&J MHP800 Deep Vein Thrombosis (DVT) Prevention System is manufactured by B&J Manufacturing , Ltd..

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.

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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.