FDA 510(k) Applications Submitted by ABBOTT DIAGNOSTICS
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K972182 | 05/29/1997 | ABBOTT STREP A CONTROLS | ABBOTT DIAGNOSTICS |
| K961439 | 04/15/1996 | ABBOTT CELL-DYN 4000 SYSTEM | ABBOTT DIAGNOSTICS |
| K964185 | 10/21/1996 | IMX CA 125 | ABBOTT DIAGNOSTICS |
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