The following data is part of a premarket notification filed by Varian Assoc., Inc. with the FDA for Brachyvision 6.0.
| Device ID | K992762 |
| 510k Number | K992762 |
| Device Name: | BRACHYVISION 6.0 |
| Classification | System, Planning, Radiation Therapy Treatment |
| 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 | MUJ |
| CFR Regulation Number | 892.5050 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1999-08-17 |
| Decision Date | 2000-03-09 |
| Summary: | summary |