Submission Details
| 510(k) Number | K100910 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | April 01, 2010 |
| Decision Date | May 11, 2011 |
| Days to Decision | 405 days |
| Submission Type | Traditional |
| Review Panel | Immunology (IM) |
| Summary | Summary PDF |
K100910 is an FDA 510(k) clearance for the IMMULITE 2000 3GALLERGY SPECIFIC IGE ASSAY KIT, MODEL L2KUN6, a System, Test, Radioallergosorbent (rast) Immunological (Class II — Special Controls, product code DHB), submitted by Siemens Medical Solutions Diagnostics (Los Angeles, US). The FDA issued a Cleared decision on May 11, 2011, 405 days after receiving the submission on April 1, 2010. This device falls under the Immunology review panel. Regulated under 21 CFR 866.5750.
| 510(k) Number | K100910 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | April 01, 2010 |
| Decision Date | May 11, 2011 |
| Days to Decision | 405 days |
| Submission Type | Traditional |
| Review Panel | Immunology (IM) |
| Summary | Summary PDF |
| Product Code | DHB — System, Test, Radioallergosorbent (rast) Immunological |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 866.5750 |