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FDA 510(k)

HEWLETT-PACKARD SERIES OF DISPOSABLE NIBP CUFFS

K-Number: K901252 · 1990-07-31

Decision Date1990-07-31
Product CodeDXQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

HEWLETT-PACKARD SERIES OF DISPOSABLE NIBP CUFFS is the device name listed in this FDA 510(k) record. The listed applicant is Hewlett-Packard Co.. It received FDA 510(k) clearance on 1990-07-31 under 510(k) number K901252. 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 HEWLETT-PACKARD SERIES OF DISPOSABLE NIBP CUFFS?

HEWLETT-PACKARD SERIES OF DISPOSABLE NIBP CUFFS is a medical device that received FDA 510(k) clearance on 1990-07-31. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K901252.

When did HEWLETT-PACKARD SERIES OF DISPOSABLE NIBP CUFFS receive FDA 510(k) clearance?

HEWLETT-PACKARD SERIES OF DISPOSABLE NIBP CUFFS received FDA 510(k) clearance on 1990-07-31, under 510(k) number K901252.

Who is the listed applicant for HEWLETT-PACKARD SERIES OF DISPOSABLE NIBP CUFFS?

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

What is the FDA product code for HEWLETT-PACKARD SERIES OF DISPOSABLE NIBP CUFFS?

The FDA product code for HEWLETT-PACKARD SERIES OF DISPOSABLE NIBP CUFFS 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 Hewlett-Packard Co. 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 230 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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