FDA 510(k) Applications Submitted by Dura Tap LLC
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K173335 | 10/23/2017 | Gazelle PTFE and Suture Delivery Device | Dura Tap LLC |
| K173644 | 11/27/2017 | Gazelle Polypropylene Suture and Delivery Device | Dura Tap LLC |
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