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FDA 510(k)

UNIMED DISPOSABLE BLOOD PRESSURE CUFF

K-Number: K120364 · 2012-05-04

Decision Date2012-05-04
Product CodeDXQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

UNIMED DISPOSABLE BLOOD PRESSURE CUFF is the device name listed in this FDA 510(k) record. The listed applicant is Unimed Medical Supplies, Inc.. It received FDA 510(k) clearance on 2012-05-04 under 510(k) number K120364. 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 UNIMED DISPOSABLE BLOOD PRESSURE CUFF?

UNIMED DISPOSABLE BLOOD PRESSURE CUFF is a medical device that received FDA 510(k) clearance on 2012-05-04. The listed applicant is Unimed Medical Supplies, Inc.. The 510(k) number is K120364.

When did UNIMED DISPOSABLE BLOOD PRESSURE CUFF receive FDA 510(k) clearance?

UNIMED DISPOSABLE BLOOD PRESSURE CUFF received FDA 510(k) clearance on 2012-05-04, under 510(k) number K120364.

Who is the listed applicant for UNIMED DISPOSABLE BLOOD PRESSURE CUFF?

The FDA 510(k) record lists Unimed Medical Supplies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for UNIMED DISPOSABLE BLOOD PRESSURE CUFF?

The FDA product code for UNIMED DISPOSABLE 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 Unimed Medical Supplies, 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 18 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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