Elegance Ferritin Elisa

FDA 510(k) K904822 · Bioclone Australia Pty , Ltd.

Substantially Equivalent

510(k) numberK904822

Submission

Device name
Elegance Ferritin Elisa
Applicant
Bioclone Australia Pty , Ltd.
Washington, DC, US
Received
October 24, 1990
Decision date
November 29, 1990
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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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More from Reference Diagnostics, Inc.

510(k)DeviceDecision
K935049Elegance Neonatal TSH ElisaJLW · Traditional 10/03/1994SE
K922284Elegance FT4 ElisaCEC · Traditional 07/10/1992SE
K910419Bioclone's Elegance Ige Elisa KitDGC · Traditional 06/21/1991SE
K910420Bioclone's Elegance HCG Elisa KitJHI · Traditional 02/26/1991SE
K905099Elegance TSH ElisaJLW · Traditional 12/18/1990SE
K905098Elegance GH ElisaCFL · Traditional 12/06/1990SE
K904387Bioclones Elegance LH Elisa KitCEP · Traditional 11/06/1990SE
K904483Elegance Prolactin ElisaCFT · Traditional 11/05/1990SE
K904405Bioclones Elegance FSH Elisa KitCGJ · Traditional 10/26/1990SE

Questions and answers

When was Elegance Ferritin Elisa cleared by the FDA?

Elegance Ferritin Elisa (K904822) received a 510(k) decision of Substantially Equivalent on November 29, 1990, 36 days after the submission was received.

What is the product code of K904822?

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