The following data is part of a premarket notification filed by Oxoid U.s.a., Inc. with the FDA for Rapid Reagin Card Test.
| Device ID | K822661 |
| 510k Number | K822661 |
| Device Name: | RAPID REAGIN CARD TEST |
| Classification | Antigens, Nontreponemal, All |
| Applicant | OXOID U.S.A., INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | GMQ |
| CFR Regulation Number | 866.3820 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-09-03 |
| Decision Date | 1982-09-21 |