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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 the device name listed in this FDA 510(k) record. The listed applicant is Honsun (Nantong) Co., Ltd.. It received FDA 510(k) clearance on 2020-04-06 under 510(k) 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. The listed applicant is Honsun (Nantong) Co., Ltd.. The 510(k) number is K192500.

When did Aneroid sphygmomanometer with stethoscope, Aneroid sphygmomanometer receive FDA 510(k) clearance?

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

Who is the listed applicant for Aneroid sphygmomanometer with stethoscope, Aneroid sphygmomanometer?

The FDA 510(k) record lists Honsun (Nantong) Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

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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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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