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FDA 510(k) Applications for Medical Device Product Code "DPG"
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FDA 510(k) Number | Applicant | Device Name | Decision Date |
K812129 | DIAGNOSTIC PRODUCTS CORP. | COAT-A-COUNT DIGITOXIN RIA KIT | 08/13/1981 |
K780075 | MILES LABORATORIES, INC. | RIALYZE DIGOXIN | 02/28/1978 |
K935229 | PB DIAGNOSTIC SYSTEMS, INC. | OPUS DIGITOXIN | 12/22/1993 |