Chrono-Log Corp.

Chrono-Log Corp. — FDA 510(k) Submissions

Chrono-Log Corp. has submitted 16 FDA 510(k) premarket notifications since 1976, of which 16 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include System, Automated Platelet Aggregation, Aggregrometer, Platelet, Reagent, Platelet Aggregation, Test, Qualitative And Quantitative Factor Deficiency, Aggregometer, Platelet, Photo-optical Scanning . Use the specialty filter in the sidebar to narrow results.