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FDA 510(k)

PROTECT ALL BLOOD PRESSURE CUFF COVER

K-Number: K964648 · 1997-02-18

Decision Date1997-02-18
Product CodeDXQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PROTECT ALL BLOOD PRESSURE CUFF COVER is the device name listed in this FDA 510(k) record. The listed applicant is Protect All, Inc.. It received FDA 510(k) clearance on 1997-02-18 under 510(k) number K964648. 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 PROTECT ALL BLOOD PRESSURE CUFF COVER?

PROTECT ALL BLOOD PRESSURE CUFF COVER is a medical device that received FDA 510(k) clearance on 1997-02-18. The listed applicant is Protect All, Inc.. The 510(k) number is K964648.

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

PROTECT ALL BLOOD PRESSURE CUFF COVER received FDA 510(k) clearance on 1997-02-18, under 510(k) number K964648.

Who is the listed applicant for PROTECT ALL BLOOD PRESSURE CUFF COVER?

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

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

The FDA product code for PROTECT ALL 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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