The following data is part of a premarket notification filed by Dms Laboratories with the FDA for Sucrose.
| Device ID | K820214 |
| 510k Number | K820214 |
| Device Name: | SUCROSE |
| Classification | Culture Media, Multiple Biochemical Test |
| Applicant | DMS LABORATORIES 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | JSE |
| CFR Regulation Number | 866.2320 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-01-26 |
| Decision Date | 1982-02-05 |