Albumin Test, Hma Albumin Test

FDA 510(k) K771259 · Hycel, Inc.

Substantially Equivalent

510(k) numberK771259

Submission

Device name
Albumin Test, Hma Albumin Test
Applicant
Hycel, Inc.
Mchenry, IL, US
Received
July 11, 1977
Decision date
August 22, 1977
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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Questions and answers

When was Albumin Test, Hma Albumin Test cleared by the FDA?

Albumin Test, Hma Albumin Test (K771259) received a 510(k) decision of Substantially Equivalent on August 22, 1977, 42 days after the submission was received.

What is the product code of K771259?

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