FDA 510(k) Applications Submitted by MAJESTIC DRUG CO., INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K964773 | 11/27/1996 | DENTEMP ONE STEP | MAJESTIC DRUG CO., INC. |
| K101771 | 06/24/2010 | RELINE-IT MODEL RELINE-IT | MAJESTIC DRUG CO., INC. |
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