Decision Date2022-10-12
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
Arm Blood Pressure Monitor is the device name listed in this FDA 510(k) record. The listed applicant is Alicn Medical Shenzhen, Inc.. It received FDA 510(k) clearance on 2022-10-12 under 510(k) number K221913. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Arm Blood Pressure Monitor?
Arm Blood Pressure Monitor is a medical device that received FDA 510(k) clearance on 2022-10-12. The listed applicant is Alicn Medical Shenzhen, Inc.. The 510(k) number is K221913.
When did Arm Blood Pressure Monitor receive FDA 510(k) clearance?
Arm Blood Pressure Monitor received FDA 510(k) clearance on 2022-10-12, under 510(k) number K221913.
Who is the listed applicant for Arm Blood Pressure Monitor?
The FDA 510(k) record lists Alicn Medical Shenzhen, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Arm Blood Pressure Monitor?
The FDA product code for Arm Blood Pressure Monitor is DXN.
Other records listing Alicn Medical Shenzhen, Inc. as applicant
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Related Devices (Code: DXN)
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.