The following data is part of a premarket notification filed by Waters Assoc., Inc. with the FDA for Model 480 Variable Wavelength Ultra Viol.
Device ID | K811975 |
510k Number | K811975 |
Device Name: | MODEL 480 VARIABLE WAVELENGTH ULTRA VIOL |
Classification | Colorimeter, Photometer, Spectrophotometer For Clinical Use |
Applicant | WATERS 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 | 1981-07-13 |
Decision Date | 1981-07-27 |