The following data is part of a premarket notification filed by Varian Assoc., Inc. with the FDA for Bds-3 Beam Data Scanner.
| Device ID | K844620 |
| 510k Number | K844620 |
| Device Name: | BDS-3 BEAM DATA SCANNER |
| Classification | Instrument, Quality-assurance, Radiologic |
| Applicant | VARIAN ASSOC., INC. 611 HANSEN WAY P.O. BOX 10800 Palo Alto, CA 94303 |
| Contact | Milton D Siegel |
| Correspondent | Milton D Siegel VARIAN ASSOC., INC. 611 HANSEN WAY P.O. BOX 10800 Palo Alto, CA 94303 |
| Product Code | LHO |
| CFR Regulation Number | 892.1940 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-11-27 |
| Decision Date | 1985-07-01 |