The following data is part of a premarket notification filed by Dms Laboratories with the FDA for Oxi.
| Device ID | K820212 |
| 510k Number | K820212 |
| Device Name: | OXI |
| Classification | Discs, Strips And Reagents, Microorganism Differentiation |
| Applicant | DMS LABORATORIES 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | JTO |
| CFR Regulation Number | 866.2660 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-01-26 |
| Decision Date | 1982-02-12 |