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FDA 510(k)

VISTA 44 GAS CHROMATOGRAPHY ANALYSIS

K-Number: K801745 · 1980-08-20

Decision Date1980-08-20
Product CodeKZQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

VISTA 44 GAS CHROMATOGRAPHY ANALYSIS is the device name listed in this FDA 510(k) record. The listed applicant is Varian Assoc., Inc.. It received FDA 510(k) clearance on 1980-08-20 under 510(k) number K801745. 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 VISTA 44 GAS CHROMATOGRAPHY ANALYSIS?

VISTA 44 GAS CHROMATOGRAPHY ANALYSIS is a medical device that received FDA 510(k) clearance on 1980-08-20. The listed applicant is Varian Assoc., Inc.. The 510(k) number is K801745.

When did VISTA 44 GAS CHROMATOGRAPHY ANALYSIS receive FDA 510(k) clearance?

VISTA 44 GAS CHROMATOGRAPHY ANALYSIS received FDA 510(k) clearance on 1980-08-20, under 510(k) number K801745.

Who is the listed applicant for VISTA 44 GAS CHROMATOGRAPHY ANALYSIS?

The FDA 510(k) record lists Varian Assoc., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VISTA 44 GAS CHROMATOGRAPHY ANALYSIS?

The FDA product code for VISTA 44 GAS CHROMATOGRAPHY ANALYSIS 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 Varian Assoc., Inc. 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 86 devices →

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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