FDA 510(k) Applications Submitted by C.R. Bard, Inc (Bard has joined BD)
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K180548 | 03/01/2018 | 3F Single Lumen and 4F Dual Lumen PowerPICC Provena Catherers; 3F Single Lumen and 4F Dual Lumen PowerPICC Provena Catherters with SOLO Valve Technology | C.R. Bard, Inc (Bard has joined BD) |
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