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FDA 510(k)

HP MODEL M1008B, NONINVASIVE BLOOD PRESSURE MODULE

K-Number: K903771 · 1991-02-19

ApplicantHewlett-Packard Co.
Decision Date1991-02-19
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

HP MODEL M1008B, NONINVASIVE BLOOD PRESSURE MODULE 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 1991-02-19 under 510(k) number K903771. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HP MODEL M1008B, NONINVASIVE BLOOD PRESSURE MODULE?

HP MODEL M1008B, NONINVASIVE BLOOD PRESSURE MODULE is a medical device that received FDA 510(k) clearance on 1991-02-19. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K903771.

When did HP MODEL M1008B, NONINVASIVE BLOOD PRESSURE MODULE receive FDA 510(k) clearance?

HP MODEL M1008B, NONINVASIVE BLOOD PRESSURE MODULE received FDA 510(k) clearance on 1991-02-19, under 510(k) number K903771.

Who is the listed applicant for HP MODEL M1008B, NONINVASIVE BLOOD PRESSURE MODULE?

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 HP MODEL M1008B, NONINVASIVE BLOOD PRESSURE MODULE?

The FDA product code for HP MODEL M1008B, NONINVASIVE BLOOD PRESSURE MODULE is DXN.

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Related Devices (Code: DXN)

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.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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