FDA 510(k) Applications Submitted by Clarus Medical, LLC
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K240535 | 02/26/2024 | Digital ClarusScope System; Digital NeuroPEN System | Clarus Medical, LLC |
| K200925 | 04/07/2020 | Clarus Peel-Away Introducer Sheath | Clarus Medical, LLC |
| K223615 | 12/05/2022 | Digital ClarusScope System, Digital NeuroPEN System | Clarus Medical, LLC |
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