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FDA 510(k)

Reusable Blood Pressure Cuff, Disposable Blood Pressure Cuff

K-Number: K173044 · 2017-11-20

Decision Date2017-11-20
Product CodeDXQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Reusable Blood Pressure Cuff, Disposable Blood Pressure Cuff is a medical device manufactured by Ningbo Albert Novosino Co., Ltd.. It received FDA 510(k) clearance on 2017-11-20 under approval number K173044. The device is classified under product code DXQ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Reusable Blood Pressure Cuff, Disposable Blood Pressure Cuff?

Reusable Blood Pressure Cuff, Disposable Blood Pressure Cuff is a medical device that received FDA 510(k) clearance on 2017-11-20. It is manufactured by Ningbo Albert Novosino Co., Ltd.. The 510(k) number is K173044.

When was Reusable Blood Pressure Cuff, Disposable Blood Pressure Cuff approved by the FDA?

Reusable Blood Pressure Cuff, Disposable Blood Pressure Cuff received FDA 510(k) clearance on 2017-11-20, under approval number K173044.

What company makes Reusable Blood Pressure Cuff, Disposable Blood Pressure Cuff?

Reusable Blood Pressure Cuff, Disposable Blood Pressure Cuff is manufactured by Ningbo Albert Novosino Co., Ltd..

What is the FDA product code for Reusable Blood Pressure Cuff, Disposable Blood Pressure Cuff?

The FDA product code for Reusable Blood Pressure Cuff, Disposable Blood Pressure Cuff is DXQ.

Related Clinical Trials

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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.