Precision Biologic, Inc.

Precision Biologic, Inc. — FDA 510(k) Submissions

Precision Biologic, Inc. has submitted 7 FDA 510(k) premarket notifications since 2004, of which 7 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Test, Qualitative And Quantitative Factor Deficiency, Test, Time, Partial Thromboplastin, Plasma, Coagulation Factor Deficient . Use the specialty filter in the sidebar to narrow results.