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FDA 510(k)

Aneroid Type Blood Pressure Kit

K-Number: K191209 · 2019-06-18

ApplicantDongguan Mars Medical Products Co., Ltd.
Decision Date2019-06-18
Product CodeDXQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Aneroid Type Blood Pressure Kit is a medical device manufactured by Dongguan Mars Medical Products Co., Ltd.. It received FDA 510(k) clearance on 2019-06-18 under approval number K191209. 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 Aneroid Type Blood Pressure Kit?

Aneroid Type Blood Pressure Kit is a medical device that received FDA 510(k) clearance on 2019-06-18. It is manufactured by Dongguan Mars Medical Products Co., Ltd.. The 510(k) number is K191209.

When was Aneroid Type Blood Pressure Kit approved by the FDA?

Aneroid Type Blood Pressure Kit received FDA 510(k) clearance on 2019-06-18, under approval number K191209.

What company makes Aneroid Type Blood Pressure Kit?

Aneroid Type Blood Pressure Kit is manufactured by Dongguan Mars Medical Products Co., Ltd..

What is the FDA product code for Aneroid Type Blood Pressure Kit?

The FDA product code for Aneroid Type Blood Pressure Kit is DXQ.

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Related PubMed Literature

PMID: 41836285 A Case Study of AI-Enabled Software as a Medical Device Cleared by the FDA for Assessing Hemorrhage Risk Index (APPRAISE-HRI) after Trauma. NEJM AI (2025) PMID: 41623865 Case Report: Hypertensive encephalopathy presents with complex types of sleep breathing events. Frontiers in cardiovascular medicine (2025)

Related Devices (Code: DXQ)

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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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