Hemohlobin A2 Control-Lyophilized

FDA 510(k) K801410 · Isolab, Inc.

Substantially Equivalent

510(k) numberK801410

Submission

Device name
Hemohlobin A2 Control-Lyophilized
Applicant
Isolab, Inc.
Mchenry, IL, US
Received
June 16, 1980
Decision date
July 21, 1980
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JPD – Hemoglobin A2 Quantitation
Device class
Class II (moderate risk)
Regulation
21 CFR 864.7400
Specialty
Hematology

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K991127Variant II B-ThalassemiaJPD · Special Bio-Rad06/10/1999SE
K924122Variant Beta-Thalassemia Short ProgramJPD · Traditional Bio-Rad03/11/1993SE
K924496Glycomat Green HBA2 Estimation Reagent KitJPD · Traditional Drew Scientific , Ltd.11/16/1992SE
K923318Columnmate Beta-Thal HBA2 Control - NormalJPD · Traditional Helena Laboratories08/25/1992SE
K923317Columnmate Beta Thal HBA2 Control-AbnormalJPD · Traditional Helena Laboratories08/25/1992SE
K913384Columnmate(Tm) Beta-Thal Cat. No. 4515JPD · Traditional Helena Laboratories12/17/1991SE
K896168Hemoglobin A2 Micro Column TestJPD · Traditional Bio-Rad01/18/1990SE
K875102Deter. of Hemoglobin A2 Using the DiamatJPD · Traditional Bio-Rad02/24/1988SE
K823870Beta Thalquik Column #5341JPD · Traditional Helena Laboratories02/01/1983SE

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K950415Fluoroscan NeonatalKHO · Traditional 09/05/1995SE
K942276Quik-Sep Quantitative Hemoglobin S AssayGIQ · Traditional 01/20/1995SE
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K944185IsoscanJQT · Traditional 11/17/1994SE
K934013Resolve Systems Alkaline Phosphatase Test KitCIN · Traditional 04/26/1994SE
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Questions and answers

When was Hemohlobin A2 Control-Lyophilized cleared by the FDA?

Hemohlobin A2 Control-Lyophilized (K801410) received a 510(k) decision of Substantially Equivalent on July 21, 1980, 35 days after the submission was received.

What is the product code of K801410?

The FDA product code is JPD – Hemoglobin A2 Quantitation, a Class II (moderate risk) device regulated under 21 CFR 864.7400.