The following data is part of a premarket notification filed by Reagent Laboratory, Inc. with the FDA for Volume Test Dye 6.
| Device ID | K841422 |
| 510k Number | K841422 |
| Device Name: | VOLUME TEST DYE 6 |
| Classification | Flame Emission Photometer For Clinical Use |
| Applicant | REAGENT LABORATORY, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | JJO |
| CFR Regulation Number | 862.2540 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-04-05 |
| Decision Date | 1984-05-11 |