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FDA 510(k) Applications for Medical Device Product Code "DPB"
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FDA 510(k) Number | Applicant | Device Name | Decision Date |
K820274 | AMERICAN DIAGNOSTIC CORP. | DIGOXIN RADIOIMMUNOASSAY | 02/23/1982 |
K821811 | CAMBRIDGE MEDICAL TECHNOLOGY | 125I DIGOXIN RADIOIMMUNOASSAY KIT | 07/02/1982 |
K771525 | DIAGNOSTIC PRODUCTS CORP. | 125 I DIGOXIN RIA KIT | 10/14/1977 |
K790602 | ENDOCRINE-METABOLIC CENTER | RIA, DIGNXIN-125-I | 07/30/1979 |
K853021 | MILES LABORATORIES, INC. | OPTIMATE DIGOXIN TEST | 08/07/1985 |
K760883 | NUCLEAR MEDICAL LABORATORIES, INC. | DIGI-TAB-RIA DIGOXIN RADIOMMUNOASSAY | 11/19/1976 |
K823014 | PCL-RIA, INC. | DIGOXIN KIT | 11/01/1982 |
K792153 | RADIOIMMUNOASSAY, INC. | DIGOXIN RADIOIMMUNOASSAY SYSTEM | 11/13/1979 |
K790540 | VENTREX LABORATORIES, INC. | RIA TEST KIT, CENTRIA DIGOXIN | 04/23/1979 |
K772306 | WIEN LABORATORIES, INC. | 125I DIGOXIN TEST SET | 12/22/1977 |