Dade Behring, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dade Behring, Inc. - FDA 510(k) Cleared Devices
Recent clearances: PT-MULTI-CALIBRATOR, MODEL OPAT07, DIMENSION VISTA SYSTEM IGG FLEX REAGENT CARTRIDGE, DIMENSION VISTA SYSTEM PROTEIN 1 CALIBRATOR, AND DIMENSION VISTA SYST, DIMENSION VISTA SYSTEM A2MAC FLEX REAGENT CARTRIDGE, DIMENSION VISTA SYSTEM PROTEIN 1 CALIBRATOR, DIMENSION VISTA SYSYEM
Dade Behring, Inc. has 343 FDA 510(k) cleared medical devices. Based in Newark,, US.
Historical record: 343 cleared submissions from 1978 to 2010.
Browse the FDA 510(k) cleared devices submitted by Dade Behring, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Dade Behring, Inc.
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