Yumizen C1200 Ferritin, Yumizen C1200 Transferrin, Yumizen C1200 Rheumatoid Factor

FDA 510(k) K191562 · Horiba Abx SAS

Substantially Equivalent

510(k) numberK191562

Submission

Device name
Yumizen C1200 Ferritin, Yumizen C1200 Transferrin, Yumizen C1200 Rheumatoid Factor
Applicant
Horiba Abx SAS
Montpellier Cedex 4, FR
Received
June 13, 2019
Decision date
March 6, 2020
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
DBF – Ferritin, Antigen, Antiserum, Control
Device class
Class II (moderate risk)
Regulation
21 CFR 866.5340
Specialty
Immunology

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Questions and answers

When was Yumizen C1200 Ferritin, Yumizen C1200 Transferrin, Yumizen C1200 Rheumatoid Factor cleared by the FDA?

Yumizen C1200 Ferritin, Yumizen C1200 Transferrin, Yumizen C1200 Rheumatoid Factor (K191562) received a 510(k) decision of Substantially Equivalent on March 6, 2020, 267 days after the submission was received.

What is the product code of K191562?

The FDA product code is DBF – Ferritin, Antigen, Antiserum, Control, a Class II (moderate risk) device regulated under 21 CFR 866.5340.