Mdi SCL-70 Test
FDA 510(k) K000934 · Micro Detect, Inc.
510(k) numberK000934
Submission
- Device name
- Mdi SCL-70 Test
- Applicant
- Micro Detect, Inc.
Tustin, CA, US - Received
- March 23, 2000
- Decision date
- April 7, 2000
- 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
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| 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 |
|---|---|---|
| K003794 | Elisa Test, SerologyLYR · Traditional | 03/30/2001SE |
| K002359 | Mdi Gliadin G TestMST · Traditional | 10/19/2000SE |
| K002358 | Mdi Gliadin a TestMST · Traditional | 10/19/2000SE |
| K000477 | Mdi Ds-Dna TestLRM · Traditional | 03/01/2000SE |
| K994029 | Mdi SM TestLLL · Traditional | 01/11/2000SE |
| K993971 | Mdi Ss-B Test Enzyme Immunoassay for the Detection of Autoantibodies to Ss-B in Human…LLL · Traditional | 01/11/2000SE |
| K993843 | Mdi RF TestDHR · Traditional | 01/11/2000SE |
| K993636 | Mdi Ss-A TestLJM · Traditional | 01/10/2000SE |
| K993635 | Mdi Sm/Rnp TestLJM · Traditional | 01/10/2000SE |
| K973508 | Pylori Detect IggLYR · Traditional | 03/10/1998SE |
Questions and answers
When was Mdi SCL-70 Test cleared by the FDA?
Mdi SCL-70 Test (K000934) received a 510(k) decision of Substantially Equivalent on April 7, 2000, 15 days after the submission was received.
What is the product code of K000934?
The FDA product code is LJM – Antinuclear Antibody (Enzyme-Labeled), Antigen, Controls, a Class II (moderate risk) device regulated under 21 CFR 866.5100.