FDA 510(k) Applications Submitted by FIONA CAMPBELL
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K011709 | 06/04/2001 | UNI-GOLD STREP A TEST KIT | TRINITY BIOTECH, PLC |
| K014233 | 12/26/2001 | CAPTIAM SYPHILIS-G ASSAY | TRINITY BIOTECH, PLC |
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