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FDA 510(k)

VARIAN 3300 & 3400 GAS CHROMATOGRAPHS

K-Number: K841891 · 1984-07-09

Decision Date1984-07-09
Product CodeKZQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

VARIAN 3300 & 3400 GAS CHROMATOGRAPHS 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 1984-07-09 under 510(k) number K841891. 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 VARIAN 3300 & 3400 GAS CHROMATOGRAPHS?

VARIAN 3300 & 3400 GAS CHROMATOGRAPHS is a medical device that received FDA 510(k) clearance on 1984-07-09. The listed applicant is Varian Assoc., Inc.. The 510(k) number is K841891.

When did VARIAN 3300 & 3400 GAS CHROMATOGRAPHS receive FDA 510(k) clearance?

VARIAN 3300 & 3400 GAS CHROMATOGRAPHS received FDA 510(k) clearance on 1984-07-09, under 510(k) number K841891.

Who is the listed applicant for VARIAN 3300 & 3400 GAS CHROMATOGRAPHS?

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 VARIAN 3300 & 3400 GAS CHROMATOGRAPHS?

The FDA product code for VARIAN 3300 & 3400 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 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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