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FDA 510(k)

NEONATAL/STERILE/DISPOS/NONINVAS BLOOD PRESS CUFF

K-Number: K905101 · 1990-12-20

ApplicantHewlett-Packard Co.
Decision Date1990-12-20
Product CodeDXQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

NEONATAL/STERILE/DISPOS/NONINVAS BLOOD PRESS CUFF 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 1990-12-20 under 510(k) number K905101. 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 NEONATAL/STERILE/DISPOS/NONINVAS BLOOD PRESS CUFF?

NEONATAL/STERILE/DISPOS/NONINVAS BLOOD PRESS CUFF is a medical device that received FDA 510(k) clearance on 1990-12-20. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K905101.

When did NEONATAL/STERILE/DISPOS/NONINVAS BLOOD PRESS CUFF receive FDA 510(k) clearance?

NEONATAL/STERILE/DISPOS/NONINVAS BLOOD PRESS CUFF received FDA 510(k) clearance on 1990-12-20, under 510(k) number K905101.

Who is the listed applicant for NEONATAL/STERILE/DISPOS/NONINVAS BLOOD PRESS CUFF?

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 NEONATAL/STERILE/DISPOS/NONINVAS BLOOD PRESS CUFF?

The FDA product code for NEONATAL/STERILE/DISPOS/NONINVAS BLOOD PRESS CUFF is DXQ.

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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.

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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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