FDA 510(k) Applications Submitted by NeuMoDx Molecular, Inc.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K230267 | 01/31/2023 | NeuMoDx CT/NG Assay 2.0 | NeuMoDx Molecular, Inc. |
| K173725 | 12/05/2017 | NeuMoDx GBS Assay | NeuMoDx Molecular, Inc. |
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