The following data is part of a premarket notification filed by Texas Immunology, Inc. with the FDA for Sero/tex Red Cell Rf Test.
| Device ID | K831597 |
| 510k Number | K831597 |
| Device Name: | SERO/TEX RED CELL RF TEST |
| Classification | System, Test, Rheumatoid Factor |
| Applicant | TEXAS IMMUNOLOGY, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | DHR |
| CFR Regulation Number | 866.5775 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-05-17 |
| Decision Date | 1983-06-30 |