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FDA 510(k) Applications for Medical Device Product Code "EBP"
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FDA 510(k) Number | Applicant | Device Name | Decision Date |
K101771 | MAJESTIC DRUG CO., INC. | RELINE-IT MODEL RELINE-IT | 09/20/2010 |
K121318 | PERMA LABORATORIES | PROSOFT | 06/06/2012 |