FDA 510(k) Applications Submitted by INNOVACON, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K061718 | 06/19/2006 | INNOVACON SPECTRUM II TEST CARD | INNOVACON, INC. |
| K062361 | 08/14/2006 | INNOVACON HCG UKTRA TEST DEVICE | INNOVACON, INC. |
| K063673 | 12/11/2006 | INNOVACON FLIPCARD FECAL OCCULT BLOOD TEST DEVICE | INNOVACON, INC. |
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