Device, Beam Limiting, X-Ray, Therapeutic

FDA product code KQA · Class II (moderate risk) · 21 CFR 892.5900 · Radiology

4510(k) clearances
0PMA approvals
0recalls

Manufacturers

510(k) clearances

510(k)DeviceApplicantDecision
K914784Papillion ProctoscopeKQA · Traditional Oldelft Corp. of America06/05/1992SE
K885126Philips RT250 Collimator (PK8050)KQA · Traditional Perkins Mfg. Co.06/01/1989SE
K844180The MCP-70-SE SystemKQA · Traditional Ellis Pharmaceutical Consulting, Inc.02/01/1985SE
K790168Collimator, BilaterialKQA · Traditional Cmsi02/15/1979SE