The following data is part of a premarket notification filed by Union Carbide Corp. with the FDA for Alizarin Sulfonate, Calcium.
| Device ID | K801290 |
| 510k Number | K801290 |
| Device Name: | ALIZARIN SULFONATE, CALCIUM |
| Classification | Alizarin Sulfonate, Calcium |
| Applicant | UNION CARBIDE CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | CID |
| CFR Regulation Number | 862.1145 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1980-05-30 |
| Decision Date | 1980-06-30 |