FDA 510(k) Applications Submitted by SHUOJIA DONG
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K011762 | 06/07/2001 | HI-WAVE; POUR-PLUS | DENPLUS, INC. |
| K991996 | 06/14/1999 | IMPACT-PLUS, IMPACT-20, DP97, DP97-20, DP-POUR AND DP-REPAIR | DENPLUS, INC. |
| K993827 | 11/12/1999 | UFI GEL HARD | VOCO GMBH |
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