FDA 510(k) Applications Submitted by DENTAL VENTURES OF AMERICA, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K000894 | 03/20/2000 | C&B RESIN PLUS POWDER/LIQUID, MODELS RETEMP A2, A3, A3.5, CL, RETEMP B2, B3, C2, D3, WH, RETEMP MO | DENTAL VENTURES OF AMERICA, INC. |
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