FDA 510(k) Applications Submitted by GENIX BIOTEK, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K971122 | 03/27/1997 | ACCULINE PREGNANCY TEST | GENIX BIOTEK, INC. |
| K964633 | 11/19/1996 | ACCUPACK PREGNANCY TEST | GENIX BIOTEK, INC. |
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