The following data is part of a premarket notification filed by Varian Assoc., Inc. with the FDA for Vista 54 Liquid Chromatography Anal. Sys.
| Device ID | K802725 |
| 510k Number | K802725 |
| Device Name: | VISTA 54 LIQUID CHROMATOGRAPHY ANAL. SYS |
| Classification | Chromatography (liquid, Gel), Clinical Use |
| Applicant | VARIAN ASSOC., INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KZR |
| CFR Regulation Number | 862.2260 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1980-10-31 |
| Decision Date | 1980-12-11 |