FDA 510(k) Applications Submitted by SYNERMED INTL., INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K983304 | 09/21/1998 | SYNERMED NEAR-INFRARED DIRECT BILIRUBIN REAGENT KIT | SYNERMED INTL., INC. |
| K974909 | 12/31/1997 | SYNERMED CREATININE REAGENT KIT | SYNERMED INTL., INC. |
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