VISTA 44 GAS CHROMATOGRAPHY ANALYSIS
K-Number: K801745 · 1980-08-20
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Device Summary
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.
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
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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