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FDA 510(k)

A&D MEDICAL LIFESOURCE DIGITAL BLOOD PRESSURE MONITORS, MODELS UB-511 & UB-512

K-Number: K042967 · 2004-12-03

ApplicantA&D Engineering, Inc.
Decision Date2004-12-03
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

A&D MEDICAL LIFESOURCE DIGITAL BLOOD PRESSURE MONITORS, MODELS UB-511 & UB-512 is the device name listed in this FDA 510(k) record. The listed applicant is A&D Engineering, Inc.. It received FDA 510(k) clearance on 2004-12-03 under 510(k) number K042967. 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 LIFESOURCE DIGITAL BLOOD PRESSURE MONITORS, MODELS UB-511 & UB-512?

A&D MEDICAL LIFESOURCE DIGITAL BLOOD PRESSURE MONITORS, MODELS UB-511 & UB-512 is a medical device that received FDA 510(k) clearance on 2004-12-03. The listed applicant is A&D Engineering, Inc.. The 510(k) number is K042967.

When did A&D MEDICAL LIFESOURCE DIGITAL BLOOD PRESSURE MONITORS, MODELS UB-511 & UB-512 receive FDA 510(k) clearance?

A&D MEDICAL LIFESOURCE DIGITAL BLOOD PRESSURE MONITORS, MODELS UB-511 & UB-512 received FDA 510(k) clearance on 2004-12-03, under 510(k) number K042967.

Who is the listed applicant for A&D MEDICAL LIFESOURCE DIGITAL BLOOD PRESSURE MONITORS, MODELS UB-511 & UB-512?

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

What is the FDA product code for A&D MEDICAL LIFESOURCE DIGITAL BLOOD PRESSURE MONITORS, MODELS UB-511 & UB-512?

The FDA product code for A&D MEDICAL LIFESOURCE DIGITAL BLOOD PRESSURE MONITORS, MODELS UB-511 & UB-512 is DXN.

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Related Devices (Code: DXN)

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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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