A & D UB-302 WRIST DIGITAL BLOOD PRESSURE MONITOR
K-Number: K960319 · 1996-07-02
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Device Summary
Frequently Asked Questions
What is the A & D UB-302 WRIST DIGITAL BLOOD PRESSURE MONITOR?
A & D UB-302 WRIST DIGITAL BLOOD PRESSURE MONITOR is a medical device that received FDA 510(k) clearance on 1996-07-02. The listed applicant is A&D Engineering, Inc.. The 510(k) number is K960319.
When did A & D UB-302 WRIST DIGITAL BLOOD PRESSURE MONITOR receive FDA 510(k) clearance?
A & D UB-302 WRIST DIGITAL BLOOD PRESSURE MONITOR received FDA 510(k) clearance on 1996-07-02, under 510(k) number K960319.
Who is the listed applicant for A & D UB-302 WRIST DIGITAL BLOOD PRESSURE MONITOR?
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 UB-302 WRIST DIGITAL BLOOD PRESSURE MONITOR?
The FDA product code for A & D UB-302 WRIST DIGITAL BLOOD PRESSURE MONITOR is DXN.
Related Clinical Trials
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.
Other records listing A&D Engineering, Inc. as applicant
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.
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.
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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