FDA 510(k) Applications Submitted by HYPERION, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K022800 | 08/23/2002 | VISIQUANT ANTI-NUCLEAR ANTIBODY TEST SYSTEM | HYPERION, INC. |
| K013213 | 09/26/2001 | HYPERION VISIQUANT ANA TEST KIT | HYPERION, INC. |
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