Rand Scientific Corp.

Rand Scientific Corp. — FDA 510(k) Submissions

Rand Scientific Corp. has submitted 10 FDA 510(k) premarket notifications since 1995, of which 10 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Lens, Contact (other Material) - Daily, Elastomer, Silicone Block, Lens, Contact (polymethylmethacrylate), Prosthesis, Chin, Internal, Implant, Muscle, Pectoralis . Use the specialty filter in the sidebar to narrow results.