The following data is part of a premarket notification filed by Theratronics, Inc. with the FDA for Theraplan Plus.
| Device ID | K954679 |
| 510k Number | K954679 |
| Device Name: | THERAPLAN PLUS |
| Classification | Accelerator, Linear, Medical |
| Applicant | THERATRONICS, INC. 413 MARCH ROAD P.O. BOX 13140 Kanata Ontario, CA K2k 2b7 |
| Contact | E. S Martell |
| Correspondent | E. S Martell THERATRONICS, INC. 413 MARCH ROAD P.O. BOX 13140 Kanata Ontario, CA K2k 2b7 |
| Product Code | IYE |
| CFR Regulation Number | 892.5050 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-10-10 |
| Decision Date | 1996-11-08 |