Varelisa Recombi Ana Profile, Model 18496
FDA 510(k) K050625 · Sweden Diagnostics (Germany) GmbH
510(k) numberK050625
Submission
- Device name
- Varelisa Recombi Ana Profile, Model 18496
- Applicant
- Sweden Diagnostics (Germany) GmbH
Freiburg, DE - Received
- March 11, 2005
- Decision date
- April 26, 2005
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- LJM – Antinuclear Antibody (Enzyme-Labeled), Antigen, Controls
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 866.5100
- Specialty
- Immunology
Other 510(k)s with product code LJM
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K182353 | EliA CENP Immunoassay, EliA U1RNP Immunoassay, EliA RNP70 ImmunoassayLJM · Traditional | Phadia AB | 11/27/2018SE |
| K151559 | ImmuLisa Enhanced Centromere Antibody ELISALJM · Traditional | Immco Diagnostics, Inc. | 03/11/2016SE |
| K140493 | Elia SCL-70S ImmunoassayLJM · Traditional | Phadia GmbH | 10/30/2014SE |
| K123880 | Quanta Flash CentromereLJM · Traditional | Inova Diagnostics, Inc. | 02/07/2014SE |
| K131330 | Gold Standard Diagnostics Anti-Nuclear Antibody (Ana) Screen Elisa Test KitLJM · Traditional | Gold Standard Diagnostics | 01/28/2014SE |
| K131185 | Ana Screen Elisa (Igg)LJM · Traditional | Euroimmun US | 07/15/2013SE |
| K083188 | Varelisa Recombi Ana Screen, Model 12 596LJM · Traditional | Phadia US, Inc. | 03/13/2009SE |
| K050967 | Varelisa Recombi CTD Screen, Model 13096LJM · Traditional | Sweden Diagnostics (Germany) GmbH | 06/28/2005SE |
| K041102 | Immulisa Antinuclear Antibody Screen ElisaLJM · Traditional | Immco Diagnostics, Inc. | 10/26/2004SE |
| K040953 | Aeskulisa Ana HEP-2LJM · Traditional | Aesku, Inc. | 06/23/2004SE |
More from Aesku, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K050967 | Varelisa Recombi CTD Screen, Model 13096LJM · Traditional | 06/28/2005SE |
| K042629 | Varelisa SM Antibodies, Model 18296LKP · Traditional | 12/08/2004SE |
| K041357 | Varelisa Gliadin Igg AntibodiesMST · Traditional | 08/02/2004SE |
| K041173 | Celikey Igg Itg Igg Antibodies, Model 17996MVM · Traditional | 08/02/2004SE |
| K041174 | Celikey TTG (Human, Recombinant) Iga Antibodies Model #18148/18196MVM · Traditional | 07/19/2004SE |
| K041354 | Varelisa Gliadin Iga Antibodies Model #19848/19896MST · Traditional | 07/16/2004SE |
| K041040 | Varelisa Mpo Anca, Model 17648/17696MOB · Traditional | 06/16/2004SE |
Questions and answers
When was Varelisa Recombi Ana Profile, Model 18496 cleared by the FDA?
Varelisa Recombi Ana Profile, Model 18496 (K050625) received a 510(k) decision of Substantially Equivalent on April 26, 2005, 46 days after the submission was received.
What is the product code of K050625?
The FDA product code is LJM – Antinuclear Antibody (Enzyme-Labeled), Antigen, Controls, a Class II (moderate risk) device regulated under 21 CFR 866.5100.