Aqueous Triolein Standards & Kits

FDA 510(k) K810742 · Supelco, Inc.

Substantially Equivalent

510(k) numberK810742

Submission

Device name
Aqueous Triolein Standards & Kits
Applicant
Supelco, Inc.
Mchenry, IL, US
Received
March 19, 1981
Decision date
March 31, 1981
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JIS – Calibrator, Primary
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1150
Specialty
Clinical Chemistry

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K881868Liquid Chromatography Columns Hisep Column & GuardDPM · Traditional 08/29/1988SE
K881361Solid Phase Extraction TubesDJY · Traditional 08/08/1988SE
K880724Liquid Chromato. ColumnsDPM · Traditional 05/27/1988SE
K874824Capillary Columns for Gas ChromatographyDII · Traditional 01/21/1988SE
K8711744-9295 Barbiturates Test MixDKB · Traditional 06/11/1987SE
K862542Capillary Columns for Gas ChromatographyDII · Traditional 08/04/1986SE
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Questions and answers

When was Aqueous Triolein Standards & Kits cleared by the FDA?

Aqueous Triolein Standards & Kits (K810742) received a 510(k) decision of Substantially Equivalent on March 31, 1981, 12 days after the submission was received.

What is the product code of K810742?

The FDA product code is JIS – Calibrator, Primary, a Class II (moderate risk) device regulated under 21 CFR 862.1150.