FDA 510(k) Applications Submitted by DIESSE DIAGNOSTICA SENESE S.P.A
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K050590 | 03/08/2005 | ENZY-WELL SYPHILIS IGG, MODEL 91106 | DIESSE DIAGNOSTICA SENESE S.P.A |
| K070062 | 01/05/2007 | COPROSET SALMONELLA AND SHIGELLA, URISET PRESERVATIVE TUBES AND SWAB SET GENERAL USE | DIESSE DIAGNOSTICA SENESE S.P.A |
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