Dako Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dako Corp. - FDA 510(k) Cleared Devices
Recent clearances: DAKO MONOCLONAL MOUSE ANTI-HUMAN PROGESTERONE RECEPTOR, CLONE PGR 636, ANTIBODY FOR IMMUNOENZYMATIC STAINING, DAKO MONOCLONAL MOUSE ANTI-HUMAN ESTROGEN RECEPTOR, DAKO MOUSE ANTI-HUMAN T-CELL, CD3/RPE-CY5, CLONE UCHT1 & DAKO MOUSE ANTI-HUMAN T-CELL, CD3/RPE, CLONE UCHT1
Dako Corp. has 54 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 54 cleared submissions from 1981 to 2002. Primary specialty: Immunology.
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FDA 510(k) Regulatory Record - Dako Corp.
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