Glycosylated Hemoglobin Kit

FDA 510(k) K801561 · Amersham Corp.

Substantially Equivalent

510(k) numberK801561

Submission

Device name
Glycosylated Hemoglobin Kit
Applicant
Amersham Corp.
Mchenry, IL, US
Received
July 8, 1980
Decision date
August 12, 1980
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
LCP – Assay, Glycosylated Hemoglobin
Device class
Class II (moderate risk)
Regulation
21 CFR 864.7470
Specialty
Hematology

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Questions and answers

When was Glycosylated Hemoglobin Kit cleared by the FDA?

Glycosylated Hemoglobin Kit (K801561) received a 510(k) decision of Substantially Equivalent on August 12, 1980, 35 days after the submission was received.

What is the product code of K801561?

The FDA product code is LCP – Assay, Glycosylated Hemoglobin, a Class II (moderate risk) device regulated under 21 CFR 864.7470.