FDA 510(k) Applications Submitted by MUREX DIAGNOSTICS, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K962028 | 05/23/1996 | WELLCOLEX E-COLI OI57 ZC60 | MUREX DIAGNOSTICS, INC. |
| K954920 | 10/26/1995 | MUREX RUB-EX | MUREX DIAGNOSTICS, INC. |
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