CVPROFILOR D0-2020 CARDIOVASCULAR PROFILING SYSTEM
K-Number: K001948 · 2000-11-01
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Device Summary
Frequently Asked Questions
What is the CVPROFILOR D0-2020 CARDIOVASCULAR PROFILING SYSTEM?
CVPROFILOR D0-2020 CARDIOVASCULAR PROFILING SYSTEM is a medical device that received FDA 510(k) clearance on 2000-11-01. The listed applicant is Hypertension Diagnostics, Inc.. The 510(k) number is K001948.
When did CVPROFILOR D0-2020 CARDIOVASCULAR PROFILING SYSTEM receive FDA 510(k) clearance?
CVPROFILOR D0-2020 CARDIOVASCULAR PROFILING SYSTEM received FDA 510(k) clearance on 2000-11-01, under 510(k) number K001948.
Who is the listed applicant for CVPROFILOR D0-2020 CARDIOVASCULAR PROFILING SYSTEM?
The FDA 510(k) record lists Hypertension Diagnostics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CVPROFILOR D0-2020 CARDIOVASCULAR PROFILING SYSTEM?
The FDA product code for CVPROFILOR D0-2020 CARDIOVASCULAR PROFILING 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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