Double Antibody Calcitonin Ria Kit

FDA 510(k) K861274 · Diagnostic Products Corp.

Substantially Equivalent

510(k) numberK861274

Submission

Device name
Double Antibody Calcitonin Ria Kit
Applicant
Diagnostic Products Corp.
Los Angeles, CA, US
Received
April 7, 1986
Decision date
June 25, 1986
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JKR – Radioimmunoassay, Calcitonin
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1140
Specialty
Clinical Chemistry

Other 510(k)s with product code JKR

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K252431Elecsys CalcitoninJKR · Traditional Roche Diagnostics GmbH04/24/2026SE
K182012ADVIA Centaur Calcitonin (CALCT) assayJKR · Traditional Axis-Shield Diagnostics Limited12/21/2018SE
K132828Elecsys Calcitonin; Immunoassay, Calset, Calcheck 5; Elecsys Precicontrol Varia 3JKR · Traditional Roche Diagnostics12/04/2013SE
K060578Calcitonin Immunoradiometric Assay (Irma) (Coated Tube Version)JKR · Traditional Scantibodies Laboratory, Inc.08/30/2006SE
K023304Immulite/Immulite 1000 Calcitonin, Model LKCL and Immulite 2000 Calcitonin, Model L2KCLJKR · Traditional Diagnostic Products Corp.12/09/2002SE
K990073CalcitoninJKR · Traditional Kmi Diagnostics, Inc.05/11/1999SE
K982491Sangui Biotech, Inc. Calcitonin Elisa KitJKR · Traditional Sangui Biotech, Inc.09/03/1998SE
K964635Nichols Advantage Chemiluminescence Calcitonin KitJKR · Traditional Nichols Institute Diagnostics05/21/1997SE
K961043Scantibodies Calcitonin Immunoradiometric Assay (Coated Bead Technology)JKR · Traditional Scantibodies Laboratory, Inc.05/06/1996SE
K945961Calcitonin Immunoassay KitJKR · Traditional Nichols Institute Diagnostics11/20/1995SE

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K023152Immulite 2000 Allergen-Specific IgeDHB · Abbreviated 12/17/2002SE
K023304Immulite/Immulite 1000 Calcitonin, Model LKCL and Immulite 2000 Calcitonin, Model L2KCLJKR · Traditional 12/09/2002SE
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Questions and answers

When was Double Antibody Calcitonin Ria Kit cleared by the FDA?

Double Antibody Calcitonin Ria Kit (K861274) received a 510(k) decision of Substantially Equivalent on June 25, 1986, 79 days after the submission was received.

What is the product code of K861274?

The FDA product code is JKR – Radioimmunoassay, Calcitonin, a Class II (moderate risk) device regulated under 21 CFR 862.1140.