VASCULAB BLOOD PRESSURE CUFF
K-Number: K831393 · 1983-06-16
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Device Summary
Frequently Asked Questions
What is the VASCULAB BLOOD PRESSURE CUFF?
VASCULAB BLOOD PRESSURE CUFF is a medical device that received FDA 510(k) clearance on 1983-06-16. The listed applicant is Medasonics, Inc.. The 510(k) number is K831393.
When did VASCULAB BLOOD PRESSURE CUFF receive FDA 510(k) clearance?
VASCULAB BLOOD PRESSURE CUFF received FDA 510(k) clearance on 1983-06-16, under 510(k) number K831393.
Who is the listed applicant for VASCULAB BLOOD PRESSURE CUFF?
The FDA 510(k) record lists Medasonics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VASCULAB BLOOD PRESSURE CUFF?
The FDA product code for VASCULAB BLOOD PRESSURE CUFF is DXQ.
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 Medasonics, 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: DXQ)
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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