FDA 510(k) Applications Submitted by Altaviz, LLC
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K231261 | 05/01/2023 | Altaviz Needle Kit II | Altaviz, LLC |
| K222681 | 09/06/2022 | Altaviz Needle Kit | Altaviz, LLC |
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