K892421 is an FDA 510(k) clearance for the MODIFIED ACCESS R-CLONE ANA/RF SCREENING TEST. This device is classified as a Antinuclear Antibody (enzyme-labeled), Antigen, Controls (Class II - Special Controls, product code LJM).
Submitted by Lipogen, Inc. (Knoxville, US). The FDA issued a Cleared decision on May 9, 1989, 29 days after receiving the submission on April 10, 1989.
This device falls under the Immunology FDA review panel. Regulated under 21 CFR 866.5100.
| 510(k) Number | K892421 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | April 10, 1989 |
| Decision Date | May 09, 1989 |
| Days to Decision | 29 days |
| Submission Type | Traditional |
| Review Panel | Immunology (IM) |
| Summary | — |
| Product Code | LJM — Antinuclear Antibody (enzyme-labeled), Antigen, Controls |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 866.5100 |