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FDA 510(k)

A & D MEDICAL UA-1000 FAMILY DAGITAL BLOOD PRESSURE MONITORS

K-Number: K111686 · 2011-08-01

ApplicantA&D Company, Ltd.
Decision Date2011-08-01
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

A & D MEDICAL UA-1000 FAMILY DAGITAL BLOOD PRESSURE MONITORS is the device name listed in this FDA 510(k) record. The listed applicant is A&D Company, Ltd.. It received FDA 510(k) clearance on 2011-08-01 under 510(k) number K111686. 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 A & D MEDICAL UA-1000 FAMILY DAGITAL BLOOD PRESSURE MONITORS?

A & D MEDICAL UA-1000 FAMILY DAGITAL BLOOD PRESSURE MONITORS is a medical device that received FDA 510(k) clearance on 2011-08-01. The listed applicant is A&D Company, Ltd.. The 510(k) number is K111686.

When did A & D MEDICAL UA-1000 FAMILY DAGITAL BLOOD PRESSURE MONITORS receive FDA 510(k) clearance?

A & D MEDICAL UA-1000 FAMILY DAGITAL BLOOD PRESSURE MONITORS received FDA 510(k) clearance on 2011-08-01, under 510(k) number K111686.

Who is the listed applicant for A & D MEDICAL UA-1000 FAMILY DAGITAL BLOOD PRESSURE MONITORS?

The FDA 510(k) record lists A&D Company, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for A & D MEDICAL UA-1000 FAMILY DAGITAL BLOOD PRESSURE MONITORS?

The FDA product code for A & D MEDICAL UA-1000 FAMILY DAGITAL BLOOD PRESSURE MONITORS is DXN.

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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.

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