FDA 510(k) Applications Submitted by Anita J. Nemeth
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K180801 | 03/28/2018 | Actreen Hi-Lite Cath, Actreen Hi-Lite Set | B. Braun Medical Inc. |
| K192577 | 09/19/2019 | Actreen Hi-Lite Intermittent Urinary Catheters | B. Braun Medical Inc. |
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