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FDA 510(k)

Aneroid Sphygmomanometer; Single Patient Use Aneroid Sphygmomanometer

K-Number: K222652 · 2022-11-28

ApplicantCardicare Company, Ltd.
Decision Date2022-11-28
Product CodeDXQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Aneroid Sphygmomanometer; Single Patient Use Aneroid Sphygmomanometer is a medical device manufactured by Cardicare Company, Ltd.. It received FDA 510(k) clearance on 2022-11-28 under approval number K222652. 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 Sphygmomanometer; Single Patient Use Aneroid Sphygmomanometer?

Aneroid Sphygmomanometer; Single Patient Use Aneroid Sphygmomanometer is a medical device that received FDA 510(k) clearance on 2022-11-28. It is manufactured by Cardicare Company, Ltd.. The 510(k) number is K222652.

When was Aneroid Sphygmomanometer; Single Patient Use Aneroid Sphygmomanometer approved by the FDA?

Aneroid Sphygmomanometer; Single Patient Use Aneroid Sphygmomanometer received FDA 510(k) clearance on 2022-11-28, under approval number K222652.

What company makes Aneroid Sphygmomanometer; Single Patient Use Aneroid Sphygmomanometer?

Aneroid Sphygmomanometer; Single Patient Use Aneroid Sphygmomanometer is manufactured by Cardicare Company, Ltd..

What is the FDA product code for Aneroid Sphygmomanometer; Single Patient Use Aneroid Sphygmomanometer?

The FDA product code for Aneroid Sphygmomanometer; Single Patient Use Aneroid Sphygmomanometer is DXQ.

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Related PubMed Literature

PMID: 42127028 Proposed standards for prosthetic foot reuse and considerations for donation of used prosthetic feet to low-and middle-income countries. PLOS global public health (2026)

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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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