Serum Albumin (BCG) Reagent Set

FDA 510(k) K860340 · Sterling Diagnostics, Inc.

Substantially Equivalent

510(k) numberK860340

Submission

Device name
Serum Albumin (BCG) Reagent Set
Applicant
Sterling Diagnostics, Inc.
Sterling Heights, MI, US
Received
January 29, 1986
Decision date
February 19, 1986
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
CIX – Bromcresol Green Dye-Binding, Albumin
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1035
Specialty
Clinical Chemistry

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More from Medica Corp.

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K921412Microprotein Reagent SetCEK · Traditional 01/21/1993SE
K914609Triglycerides Reagent SetCDT · Traditional 11/07/1991SE
K914039Sodium Reagent SetCEI · Traditional 10/31/1991SE
K914040Phospholipid Reagent SetJNT · Traditional 10/30/1991SE
K862255Lactate Dehydrogenase (LDH) Reagent Set (UV Rate)CFJ · Traditional 07/29/1986SE
K861962Vanilmandelic Acid (Vma) Reagent SetCDF · Traditional 07/07/1986SE
K862256Alkaline Phosphatase (PNPP Rate) Reagent SetCJE · Traditional 07/01/1986SE
K862210Urea Nitrogen (GLDH) Reagent Set (UV)CDQ · Traditional 07/01/1986SE
K862209Alt (SGPT) Reagent Set (UV Rate)CKA · Traditional 06/25/1986SE
K861855Hydroxybutyrate Dehydrogenase (HBD) Reagent SetJKF · Traditional 06/16/1986SE

Questions and answers

When was Serum Albumin (BCG) Reagent Set cleared by the FDA?

Serum Albumin (BCG) Reagent Set (K860340) received a 510(k) decision of Substantially Equivalent on February 19, 1986, 21 days after the submission was received.

What is the product code of K860340?

The FDA product code is CIX – Bromcresol Green Dye-Binding, Albumin, a Class II (moderate risk) device regulated under 21 CFR 862.1035.