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FDA 510(k)

5880 SERIES OF GAS CHROMATOGRAPHS

K-Number: K791138 · 1979-07-24

Decision Date1979-07-24
Product CodeKZQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

5880 SERIES OF GAS CHROMATOGRAPHS 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 1979-07-24 under 510(k) number K791138. The device is classified under product code KZQ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 5880 SERIES OF GAS CHROMATOGRAPHS?

5880 SERIES OF GAS CHROMATOGRAPHS is a medical device that received FDA 510(k) clearance on 1979-07-24. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K791138.

When did 5880 SERIES OF GAS CHROMATOGRAPHS receive FDA 510(k) clearance?

5880 SERIES OF GAS CHROMATOGRAPHS received FDA 510(k) clearance on 1979-07-24, under 510(k) number K791138.

Who is the listed applicant for 5880 SERIES OF GAS CHROMATOGRAPHS?

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 5880 SERIES OF GAS CHROMATOGRAPHS?

The FDA product code for 5880 SERIES OF GAS CHROMATOGRAPHS is KZQ.

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.

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Related Devices (Code: KZQ)

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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