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FDA 510(k)

Aneroid Sphygmomanometer

K-Number: K230859 · 2023-06-28

ApplicantWenzhou Kangshun Medical Devices Co.,Ltd
Decision Date2023-06-28
Product CodeDXQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Aneroid Sphygmomanometer is the device name listed in this FDA 510(k) record. The listed applicant is Wenzhou Kangshun Medical Devices Co.,Ltd. It received FDA 510(k) clearance on 2023-06-28 under 510(k) number K230859. 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?

Aneroid Sphygmomanometer is a medical device that received FDA 510(k) clearance on 2023-06-28. The listed applicant is Wenzhou Kangshun Medical Devices Co.,Ltd. The 510(k) number is K230859.

When did Aneroid Sphygmomanometer receive FDA 510(k) clearance?

Aneroid Sphygmomanometer received FDA 510(k) clearance on 2023-06-28, under 510(k) number K230859.

Who is the listed applicant for Aneroid Sphygmomanometer?

The FDA 510(k) record lists Wenzhou Kangshun Medical Devices Co.,Ltd as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Aneroid Sphygmomanometer?

The FDA product code for Aneroid Sphygmomanometer is DXQ.

Related Devices (Code: DXQ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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.

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