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FDA 510(k)

A&D MEDICAL TM-2430 AND TM-2431 AMBULATORY BLOOD PRESSURE

K-Number: K992808 · 1999-09-01

ApplicantA&D Medical Div.
Decision Date1999-09-01
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

A&D MEDICAL TM-2430 AND TM-2431 AMBULATORY BLOOD PRESSURE is the device name listed in this FDA 510(k) record. The listed applicant is A&D Medical Div.. It received FDA 510(k) clearance on 1999-09-01 under 510(k) number K992808. 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 TM-2430 AND TM-2431 AMBULATORY BLOOD PRESSURE?

A&D MEDICAL TM-2430 AND TM-2431 AMBULATORY BLOOD PRESSURE is a medical device that received FDA 510(k) clearance on 1999-09-01. The listed applicant is A&D Medical Div.. The 510(k) number is K992808.

When did A&D MEDICAL TM-2430 AND TM-2431 AMBULATORY BLOOD PRESSURE receive FDA 510(k) clearance?

A&D MEDICAL TM-2430 AND TM-2431 AMBULATORY BLOOD PRESSURE received FDA 510(k) clearance on 1999-09-01, under 510(k) number K992808.

Who is the listed applicant for A&D MEDICAL TM-2430 AND TM-2431 AMBULATORY BLOOD PRESSURE?

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

What is the FDA product code for A&D MEDICAL TM-2430 AND TM-2431 AMBULATORY BLOOD PRESSURE?

The FDA product code for A&D MEDICAL TM-2430 AND TM-2431 AMBULATORY BLOOD PRESSURE 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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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