FDA 510(k) Applications Submitted by Venocare, Inc.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K243105 | 09/30/2024 | Ruby Intravascular Catheter | Venocare, Inc. |
| K244047 | 12/31/2024 | NaviÖ Needle-free Blood Collection Device (VNC20500FG, VNC22500FG, VNC24500FG) | Venocare, Inc. |
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