Sepratech Corporation C/O Keller and Heckman is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sepratech Corporation C/O Keller and Heckman - FDA 510(k) Cleared Dev...
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Sepratech Corporation C/O Keller and Heckman has 1 FDA 510(k) cleared medical devices. Based in Washington, US.
Historical record: 1 cleared submissions from 1986 to 1986. Primary specialty: Hematology.
Browse the FDA 510(k) cleared devices submitted by Sepratech Corporation C/O Keller and Heckman Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Sepratech Corporation C/O Keller and Heckman
1 devices