The following data is part of a premarket notification filed by Oxoid U.s.a., Inc. with the FDA for Thymine/thymidine Discs Ddg.
| Device ID | K830939 |
| 510k Number | K830939 |
| Device Name: | THYMINE/THYMIDINE DISCS DDG |
| Classification | Discs, Strips And Reagents, Microorganism Differentiation |
| Applicant | OXOID U.S.A., INC. 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 | 1983-03-24 |
| Decision Date | 1983-04-13 |