FDA 510(k) Applications for Medical Device Product Code "DND"
(Radioimmunoassay, Digitoxin (125-I), Rabbit Antibody, Solid Phase Sep.)

FDA 510(k) Number Applicant Device Name Decision Date
K760077 SMITH KLINE DIAGNOSTICS, INC. TEST, RIA, SERUM DIGOXIN 07/16/1976


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