The following data is part of a premarket notification filed by Varian Assoc., Inc. with the FDA for Varian 2000 Liquid Chromatography Analy.
| Device ID | K841890 |
| 510k Number | K841890 |
| Device Name: | VARIAN 2000 LIQUID CHROMATOGRAPHY ANALY |
| 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 | 1984-05-07 |
| Decision Date | 1984-06-14 |