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FDA 510(k)

Aneroid Sphygmomanometer with Stethoscope; Aneroid Sphygmomanometer

K-Number: K240165 · 2024-03-20

ApplicantWenzhou Longwan Medical Device Factory
Decision Date2024-03-20
Product CodeDXQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Aneroid Sphygmomanometer with Stethoscope; Aneroid Sphygmomanometer is a medical device manufactured by Wenzhou Longwan Medical Device Factory. It received FDA 510(k) clearance on 2024-03-20 under approval number K240165. 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 with Stethoscope; Aneroid Sphygmomanometer?

Aneroid Sphygmomanometer with Stethoscope; Aneroid Sphygmomanometer is a medical device that received FDA 510(k) clearance on 2024-03-20. It is manufactured by Wenzhou Longwan Medical Device Factory. The 510(k) number is K240165.

When was Aneroid Sphygmomanometer with Stethoscope; Aneroid Sphygmomanometer approved by the FDA?

Aneroid Sphygmomanometer with Stethoscope; Aneroid Sphygmomanometer received FDA 510(k) clearance on 2024-03-20, under approval number K240165.

What company makes Aneroid Sphygmomanometer with Stethoscope; Aneroid Sphygmomanometer?

Aneroid Sphygmomanometer with Stethoscope; Aneroid Sphygmomanometer is manufactured by Wenzhou Longwan Medical Device Factory.

What is the FDA product code for Aneroid Sphygmomanometer with Stethoscope; Aneroid Sphygmomanometer?

The FDA product code for Aneroid Sphygmomanometer with Stethoscope; Aneroid Sphygmomanometer is 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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