The following data is part of a premarket notification filed by Oxoid U.s.a., Inc. with the FDA for Wilkins-chalgren Anaerobe Agar.
| Device ID | K811513 |
| 510k Number | K811513 |
| Device Name: | WILKINS-CHALGREN ANAEROBE AGAR |
| Classification | Culture Media, Antimicrobial Susceptibility Test, Excluding Mueller Hinton Agar |
| Applicant | OXOID U.S.A., INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | JSO |
| CFR Regulation Number | 866.1700 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-05-28 |
| Decision Date | 1981-06-18 |