Model 5790 Gas Chromatograph

FDA 510(k) K820071 · Hewlett-Packard Co.

Substantially Equivalent

510(k) numberK820071

Submission

Device name
Model 5790 Gas Chromatograph
Applicant
Hewlett-Packard Co.
Mchenry, IL, US
Received
January 12, 1982
Decision date
January 28, 1982
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
KZQ – Chromatography(Gas), Clinical Use
Device class
Class I (low risk)
Regulation
21 CFR 862.2250
Specialty
Clinical Chemistry

Other 510(k)s with product code KZQ

510(k)DeviceApplicantDecision
K8721228000 Series Gas ChromatographsKZQ · Traditional The Perkin-Elmer Corp.06/17/1987SE
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K832962Gas Chromatograph 5890AKZQ · Traditional Hewlett-Packard Co.10/28/1983SE
K831387HS-100 Headspace Sampling AccessoryKZQ · Traditional The Perkin-Elmer Corp.08/24/1983SE
K830147Sigma 300 Gas ChromatrographKZQ · Traditional The Perkin-Elmer Corp.02/07/1983SE
K820283Sigma 2000 Gas ChromatographKZQ · Traditional The Perkin-Elmer Corp.02/23/1982SE
K820025Trace Analytical Reduction Gas AnalyzKZQ · Traditional Trace Analytical02/15/1982SE
K801745Vista 44 Gas Chromatography AnalysisKZQ · Traditional Varian Assoc., Inc.08/20/1980SE
K7911385880 Series of Gas ChromatographsKZQ · Traditional Hewlett-Packard Co.07/24/1979SE
K770639Detector, Ir, Model GC-33KZQ · Traditional Peokin-Elmer Corp.06/24/1977SE

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Questions and answers

When was Model 5790 Gas Chromatograph cleared by the FDA?

Model 5790 Gas Chromatograph (K820071) received a 510(k) decision of Substantially Equivalent on January 28, 1982, 16 days after the submission was received.

What is the product code of K820071?

The FDA product code is KZQ – Chromatography(Gas), Clinical Use, a Class I (low risk) device regulated under 21 CFR 862.2250.