FDA 510(k) Applications Submitted by KENNETH T BURCK
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K972053 | 06/02/1997 | PIXI YOUNG ADULT REFERENC POPULATION FOR OS CALCIS AND FOREARM | LUNAR CORP. |
| K001590 | 05/17/2000 | DND 101 | UROGYN LTD. |
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