NONINVASIVE BLOOD PRESSURE MEASUREMENT SYSTEM
K-Number: K002791 · 2001-01-29
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Device Summary
Frequently Asked Questions
What is the NONINVASIVE BLOOD PRESSURE MEASUREMENT SYSTEM?
NONINVASIVE BLOOD PRESSURE MEASUREMENT SYSTEM is a medical device that received FDA 510(k) clearance on 2001-01-29. The listed applicant is Unix Electronic Co. , Ltd.. The 510(k) number is K002791.
When did NONINVASIVE BLOOD PRESSURE MEASUREMENT SYSTEM receive FDA 510(k) clearance?
NONINVASIVE BLOOD PRESSURE MEASUREMENT SYSTEM received FDA 510(k) clearance on 2001-01-29, under 510(k) number K002791.
Who is the listed applicant for NONINVASIVE BLOOD PRESSURE MEASUREMENT SYSTEM?
The FDA 510(k) record lists Unix Electronic Co. , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NONINVASIVE BLOOD PRESSURE MEASUREMENT SYSTEM?
The FDA product code for NONINVASIVE BLOOD PRESSURE MEASUREMENT SYSTEM 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.
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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