The following data is part of a premarket notification filed by Varian Assoc., Inc. with the FDA for Somavision.
| Device ID | K992751 |
| 510k Number | K992751 |
| Device Name: | SOMAVISION |
| Classification | System, Simulation, Radiation Therapy |
| Applicant | VARIAN ASSOC., INC. 3045 HANOVER ST. Palo Alto, CA 94304 -1129 |
| Contact | Linda S Nash |
| Correspondent | Linda S Nash VARIAN ASSOC., INC. 3045 HANOVER ST. Palo Alto, CA 94304 -1129 |
| Product Code | KPQ |
| CFR Regulation Number | 892.5840 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1999-08-16 |
| Decision Date | 2000-02-16 |
| Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() SOMAVISION 78240593 2862726 Dead/Cancelled |
Nellans, Neal 2003-04-22 |
![]() SOMAVISION 75231777 2324737 Dead/Cancelled |
VARIAN MEDICAL SYSTEMS TECHNOLOGIES, INC. 1997-01-27 |