AUTOMATIC DIGITAL BLOOD PRESSURE MONITOR
K-Number: K942336 · 1994-11-28
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Device Summary
Frequently Asked Questions
What is the AUTOMATIC DIGITAL BLOOD PRESSURE MONITOR?
AUTOMATIC DIGITAL BLOOD PRESSURE MONITOR is a medical device that received FDA 510(k) clearance on 1994-11-28. The listed applicant is Integrated Display Technology, Ltd.. The 510(k) number is K942336.
When did AUTOMATIC DIGITAL BLOOD PRESSURE MONITOR receive FDA 510(k) clearance?
AUTOMATIC DIGITAL BLOOD PRESSURE MONITOR received FDA 510(k) clearance on 1994-11-28, under 510(k) number K942336.
Who is the listed applicant for AUTOMATIC DIGITAL BLOOD PRESSURE MONITOR?
The FDA 510(k) record lists Integrated Display Technology, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AUTOMATIC DIGITAL BLOOD PRESSURE MONITOR?
The FDA product code for AUTOMATIC 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 Integrated Display Technology, Ltd. 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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