Autostat II Anti-Sm/Rnp Elisa

FDA 510(k) K990624 · Cogent Diagnotics , Ltd.

Substantially Equivalent

510(k) numberK990624

Submission

Device name
Autostat II Anti-Sm/Rnp Elisa
Applicant
Cogent Diagnotics , Ltd.
Midlothian, Scotland, GB
Received
February 25, 1999
Decision date
April 28, 1999
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
LKO – Anti-Rnp Antibody, Antigen And Control
Device class
Class II (moderate risk)
Regulation
21 CFR 866.5100
Specialty
Immunology

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K022017Rhigene MESACUP-2 Test RNP, Model M7741LKO · Traditional Rhigene, Inc.08/14/2002SE
K000752Rhigene MESACUP2 Test- RNPLKO · Traditional Rhigene, Inc.05/09/2000SE
K993589Varelisa RNP AntibodiesLKO · Traditional Pharmacia & Upjohn Co.11/26/1999SE
K984476Liquichek Anti-Rnp Control, Eia, Model 207LKO · Traditional Bio-Rad12/22/1998SE
K983465The Aptus (Automated) Application of the Sm/Rnp Elisa Test System. an Enzyme Linked…LKO · Traditional Zeus Scientific, Inc.11/18/1998SE

More from Zeus Scientific, Inc.

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K003057Autostat II ENA-4 Profile ElisaLLL · Traditional 10/13/2000SE
K003054Autostat II ENA-6 Profile ElisaLLL · Traditional 10/13/2000SE
K002215Autostat II Anti-Myeloperoxidase (Mpo) ElisaMOB · Traditional 09/28/2000SE
K993557Autostat II Rheumatoid Factor Iga ElisaDHR · Traditional 03/03/2000SE
K994338Autostat II Rheumatoid Factor Igm ElisaDHR · Traditional 02/03/2000SE
K993085Autostat II Anti-Cardiolipin Screen ElisaMID · Traditional 02/01/2000SE
K993304Autostat II Rheumatoid Factor Igg ElisaDHR · Traditional 12/06/1999SE
K992449Autostat II Anti-Cardiolipin Igm ElisaMID · Traditional 11/24/1999SE
K993087Autostat II Anti-Gliadin Igg ElisaMST · Traditional 11/12/1999SE
K993086Autostat II Anti-Gliadin Iga ElisaMST · Traditional 11/12/1999SE

Questions and answers

When was Autostat II Anti-Sm/Rnp Elisa cleared by the FDA?

Autostat II Anti-Sm/Rnp Elisa (K990624) received a 510(k) decision of Substantially Equivalent on April 28, 1999, 62 days after the submission was received.

What is the product code of K990624?

The FDA product code is LKO – Anti-Rnp Antibody, Antigen And Control, a Class II (moderate risk) device regulated under 21 CFR 866.5100.