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FDA 510(k)

CUFF, BLOOD PRESSURE

K-Number: K902132 · 1990-06-29

Decision Date1990-06-29
Product CodeDXQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CUFF, BLOOD PRESSURE is the device name listed in this FDA 510(k) record. The listed applicant is Buffalo Medical Specialties Mfg., Inc.. It received FDA 510(k) clearance on 1990-06-29 under 510(k) number K902132. 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 CUFF, BLOOD PRESSURE?

CUFF, BLOOD PRESSURE is a medical device that received FDA 510(k) clearance on 1990-06-29. The listed applicant is Buffalo Medical Specialties Mfg., Inc.. The 510(k) number is K902132.

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

CUFF, BLOOD PRESSURE received FDA 510(k) clearance on 1990-06-29, under 510(k) number K902132.

Who is the listed applicant for CUFF, BLOOD PRESSURE?

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

What is the FDA product code for CUFF, BLOOD PRESSURE?

The FDA product code for CUFF, BLOOD PRESSURE 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 Buffalo Medical Specialties Mfg., 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

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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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