FDA 510(k) Applications Submitted by CONSTANCE A FINCH
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K980120 | 01/13/1998 | DIGENE DML 2000 MICROPLATE LUMINOMETER | DIGENE CORP. |
| K971586 | 05/01/1997 | DIGENE CERVICAL BRUSH | DIGENE CORP. |
| K974901 | 12/31/1997 | HYBRID CAPTURE SYSTEM CMV DNA ASSAY | DIGENE CORP. |
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