Submission Details
| 510(k) Number | K990624 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | February 25, 1999 |
| Decision Date | April 28, 1999 |
| Days to Decision | 62 days |
| Submission Type | Traditional |
| Review Panel | Immunology (IM) |
| Summary | Statement |
K990624 is an FDA 510(k) clearance for the AUTOSTAT II ANTI-SM/RNP ELISA, a Anti-rnp Antibody, Antigen And Control (Class II — Special Controls, product code LKO), submitted by Cogent Diagnotics , Ltd. (Midlothian, Scotland, GB). The FDA issued a Cleared decision on April 28, 1999, 62 days after receiving the submission on February 25, 1999. This device falls under the Immunology review panel. Regulated under 21 CFR 866.5100.
| 510(k) Number | K990624 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | February 25, 1999 |
| Decision Date | April 28, 1999 |
| Days to Decision | 62 days |
| Submission Type | Traditional |
| Review Panel | Immunology (IM) |
| Summary | Statement |
| Product Code | LKO — Anti-rnp Antibody, Antigen And Control |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 866.5100 |