Quest Intl., Inc.

Quest Intl., Inc. — FDA 510(k) Submissions

Quest Intl., Inc. has submitted 25 FDA 510(k) premarket notifications since 1989, of which 25 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Epstein-barr Virus, Other, Latex Patient Examination Glove, Enzyme Linked Immunoabsorbent Assay, Cytomegalovirus, Enzyme Linked Immunoabsorbent Assay, Toxoplasma Gondii, Enzyme Linked Immunoabsorbent Assay, Rubella . Use the specialty filter in the sidebar to narrow results.