General Atomics

General Atomics — FDA 510(k) Submissions

General Atomics has submitted 6 FDA 510(k) premarket notifications since 2003, of which 6 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Atomic Absorption, Lithium, Single (specified) Analyte Controls (assayed And Unassayed), Assay, Glycosylated Hemoglobin, Ldl & Vldl Precipitation, Hdl, Apolipoproteins . Use the specialty filter in the sidebar to narrow results.