Deka Research & Development Corp.

Deka Research & Development Corp. — FDA 510(k) Submissions

Deka Research & Development Corp. has submitted 10 FDA 510(k) premarket notifications since 1984, of which 10 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Controller, Infusion, Intravascular, Electronic, System, Peritoneal, Automatic Delivery, Alternate Controller Enabled Insulin Infusion Pump, Set, Administration, Intravascular, Clamp, Tubing, Blood, Automatic . Use the specialty filter in the sidebar to narrow results.