Femspec LLC

Femspec LLC — FDA 510(k) Submissions

Femspec LLC has submitted 4 FDA 510(k) premarket notifications since 2004, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Speculum, Vaginal, Nonmetal, Curette, Suction, Endometrial (and Accessories), Sampler, Endocervical . Use the specialty filter in the sidebar to narrow results.