FDA 510(k) Applications Submitted by DRFP LTD
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K100248 | 01/27/2010 | DRFP PROSMART ROOT CANAL OBTURATION SYSTEM, PROPOINTS 4% 6%, PT, S | DRFP LTD |
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