Abbott Vision(Tm) Glycated HB

FDA 510(k) K904027 · Abbott Laboratories

Substantially Equivalent

510(k) numberK904027

Submission

Device name
Abbott Vision(Tm) Glycated HB
Applicant
Abbott Laboratories
Abbott Park, IL, US
Received
August 30, 1990
Decision date
February 7, 1991
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 Abbott Vision(Tm) Glycated HB cleared by the FDA?

Abbott Vision(Tm) Glycated HB (K904027) received a 510(k) decision of Substantially Equivalent on February 7, 1991, 161 days after the submission was received.

What is the product code of K904027?

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