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FDA 510(k)

Aneroid sphygmomanometer with stethoscope, Aneroid sphygmomanometer

K-Number: K192500 · 2020-04-06

ApplicantHonsun (Nantong) Co., Ltd.
Decision Date2020-04-06
Product CodeDXQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Aneroid sphygmomanometer with stethoscope, Aneroid sphygmomanometer is a medical device manufactured by Honsun (Nantong) Co., Ltd.. It received FDA 510(k) clearance on 2020-04-06 under approval number K192500. 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 2020-04-06. It is manufactured by Honsun (Nantong) Co., Ltd.. The 510(k) number is K192500.

When was Aneroid sphygmomanometer with stethoscope, Aneroid sphygmomanometer approved by the FDA?

Aneroid sphygmomanometer with stethoscope, Aneroid sphygmomanometer received FDA 510(k) clearance on 2020-04-06, under approval number K192500.

What company makes Aneroid sphygmomanometer with stethoscope, Aneroid sphygmomanometer?

Aneroid sphygmomanometer with stethoscope, Aneroid sphygmomanometer is manufactured by Honsun (Nantong) Co., Ltd..

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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