The following data is part of a premarket notification filed by Varian Assoc., Inc. with the FDA for Model Dms 100 Ultraviolet-visible Spec.
Device ID | K831866 |
510k Number | K831866 |
Device Name: | MODEL DMS 100 ULTRAVIOLET-VISIBLE SPEC |
Classification | Colorimeter, Photometer, Spectrophotometer For Clinical Use |
Applicant | VARIAN ASSOC., INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | JJQ |
CFR Regulation Number | 862.2300 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1983-06-10 |
Decision Date | 1983-07-28 |