Submission Details
| 510(k) Number | K082085 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | July 23, 2008 |
| Decision Date | April 17, 2009 |
| Days to Decision | 268 days |
| Submission Type | Traditional |
| Review Panel | Immunology (IM) |
| Summary | Statement |
K082085 is an FDA 510(k) clearance for the CAPILLARYS IMMUNOTYPING, MODEL 2100, a Immunoelectrophoretic, Immunoglobulins, (g, A, M) (Class II — Special Controls, product code CFF), submitted by Sebia (Norcross, US). The FDA issued a Cleared decision on April 17, 2009, 268 days after receiving the submission on July 23, 2008. This device falls under the Immunology review panel. Regulated under 21 CFR 866.5510.
| 510(k) Number | K082085 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | July 23, 2008 |
| Decision Date | April 17, 2009 |
| Days to Decision | 268 days |
| Submission Type | Traditional |
| Review Panel | Immunology (IM) |
| Summary | Statement |
| Product Code | CFF — Immunoelectrophoretic, Immunoglobulins, (g, A, M) |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 866.5510 |