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FDA 510(k)

VASCULAB BLOOD PRESSURE CUFF

K-Number: K831393 · 1983-06-16

Decision Date1983-06-16
Product CodeDXQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VASCULAB BLOOD PRESSURE CUFF is the device name listed in this FDA 510(k) record. The listed applicant is Medasonics, Inc.. It received FDA 510(k) clearance on 1983-06-16 under 510(k) number K831393. The device is classified under product code DXQ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 19 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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