The following data is part of a premarket notification filed by Computerized Medical Systems, Inc. with the FDA for Radiation Beam Data Acquistioin Systems.
Device ID | K854880 |
510k Number | K854880 |
Device Name: | RADIATION BEAM DATA ACQUISTIOIN SYSTEMS |
Classification | System, Simulation, Radiation Therapy |
Applicant | COMPUTERIZED MEDICAL SYSTEMS, INC. 2294 WELDON PKWY. St. Louis, MO 63146 |
Contact | Melvin Mccollum |
Correspondent | Melvin Mccollum COMPUTERIZED MEDICAL SYSTEMS, INC. 2294 WELDON PKWY. St. Louis, MO 63146 |
Product Code | KPQ |
CFR Regulation Number | 892.5840 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1985-12-06 |
Decision Date | 1986-01-10 |