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FDA 510(k)

BLOOD PRESSURE CUFF COVER

K-Number: K781671 · 1978-11-16

Decision Date1978-11-16
Product CodeDXQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BLOOD PRESSURE CUFF COVER is the device name listed in this FDA 510(k) record. The listed applicant is David Cott Co.. It received FDA 510(k) clearance on 1978-11-16 under 510(k) number K781671. 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 BLOOD PRESSURE CUFF COVER?

BLOOD PRESSURE CUFF COVER is a medical device that received FDA 510(k) clearance on 1978-11-16. The listed applicant is David Cott Co.. The 510(k) number is K781671.

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

BLOOD PRESSURE CUFF COVER received FDA 510(k) clearance on 1978-11-16, under 510(k) number K781671.

Who is the listed applicant for BLOOD PRESSURE CUFF COVER?

The FDA 510(k) record lists David Cott Co. as the applicant. This does not by itself establish the device manufacturer.

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

The FDA product code for BLOOD PRESSURE CUFF COVER 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.

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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