FDA 510(k) Applications Submitted by UROGYN LTD.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K014248 | 12/26/2001 | DND 202 MANUAL UROLOGICAL DIGITAL NEEDLE DRIVER | UROGYN LTD. |
| K001590 | 05/17/2000 | DND 101 | UROGYN LTD. |
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