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FDA 510(k)

FLUID MEASUREMENT STAND

K-Number: K790365 · 1979-05-11

ApplicantHewlett-Packard Co.
Decision Date1979-05-11
Product CodeFFG
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

FLUID MEASUREMENT STAND 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 1979-05-11 under 510(k) number K790365. The device is classified under product code FFG. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLUID MEASUREMENT STAND?

FLUID MEASUREMENT STAND is a medical device that received FDA 510(k) clearance on 1979-05-11. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K790365.

When did FLUID MEASUREMENT STAND receive FDA 510(k) clearance?

FLUID MEASUREMENT STAND received FDA 510(k) clearance on 1979-05-11, under 510(k) number K790365.

Who is the listed applicant for FLUID MEASUREMENT STAND?

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 FLUID MEASUREMENT STAND?

The FDA product code for FLUID MEASUREMENT STAND is FFG.

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Other records listing Hewlett-Packard Co. as applicant

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Related Devices (Code: FFG)

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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