FDA 510(k) Applications Submitted by ORGENTEC DIAGNOSTIKA GMBH
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K100499 | 02/22/2010 | ORGENTEC RHEUMATOID FACTOR EIA | ORGENTEC DIAGNOSTIKA GMBH |
| K092399 | 08/06/2009 | ANTI-MUTATED CITRULLINATED VIMENTIN EIA | ORGENTEC DIAGNOSTIKA GMBH |
| K030929 | 03/24/2003 | ANA DETECT | ORGENTEC DIAGNOSTIKA GMBH |
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