Amizyme-Ana Test Kit
FDA 510(k) K842532 · Amico Lab, Inc.
510(k) numberK842532
Submission
- Device name
- Amizyme-Ana Test Kit
- Applicant
- Amico Lab, Inc.
Mchenry, IL, US - Received
- June 28, 1984
- Decision date
- September 20, 1984
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
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 |
| K050625 | Varelisa Recombi Ana Profile, Model 18496LJM · Traditional | Sweden Diagnostics (Germany) GmbH | 04/26/2005SE |
| K041102 | Immulisa Antinuclear Antibody Screen ElisaLJM · Traditional | Immco Diagnostics, Inc. | 10/26/2004SE |
More from Immco Diagnostics, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K842662 | Anti-Epstein-Barr Virus KitGNP · Traditional | 12/12/1985SE |
| K842663 | Anti-Herpes Simplex Virus Type 1 or 2GQO · Traditional | 12/06/1985SE |
| K842661 | Anti-Cytomegalovirus KitGQI · Traditional | 12/06/1985SE |
| K842531 | Amizyme-Hsv Types 1 & 2 Test KitsGQO · Traditional | 12/06/1985SE |
| K842530 | Amizyme-Ebv Test KitGNP · Traditional | 12/06/1985SE |
| K842529 | Amizyme-Cmv KitGQI · Traditional | 12/06/1985SE |
| K842660 | Anti-Schistosoma Species KitGNH · Traditional | 10/30/1984SE |
| K842658 | Anti-Chlamydia Trachomatis KitLJP · Traditional | 10/01/1984SE |
| K842525 | Amizyme-C Trachomatis Test KitLJP · Traditional | 10/01/1984SE |
| K842533 | Amizyme-Andna Test KitLJM · Traditional | 09/20/1984SE |
Questions and answers
When was Amizyme-Ana Test Kit cleared by the FDA?
Amizyme-Ana Test Kit (K842532) received a 510(k) decision of Substantially Equivalent on September 20, 1984, 84 days after the submission was received.
What is the product code of K842532?
The FDA product code is LJM – Antinuclear Antibody (Enzyme-Labeled), Antigen, Controls, a Class II (moderate risk) device regulated under 21 CFR 866.5100.