FDA 510(k) Applications Submitted by Nancy Xu
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K182337 | 08/28/2018 | HYBRID Guidewire | Balt USA, LLC |
| K183045 | 11/02/2018 | Eclipse 2L | Balt USA, LLC |
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