FDA 510(k) Applications Submitted by RHODA FILIPINA
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K981106 | 03/26/1998 | UREA NITROGEN (BUN) LIQUID REAGENT | TECO DIAGNOSTICS |
| K981650 | 05/11/1998 | AST/SGOT LIQUID REAGENT - KINETIC METHOD | TECO DIAGNOSTICS |
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