The following data is part of a premarket notification filed by Immunostics, Inc. with the FDA for Rheumacol Rheumatoid Factor Test.
| Device ID | K972456 |
| 510k Number | K972456 |
| Device Name: | RHEUMACOL RHEUMATOID FACTOR TEST |
| Classification | System, Test, Rheumatoid Factor |
| Applicant | IMMUNOSTICS, INC. 3505 SUNSET AVE. Ocean, NJ 07712 |
| Contact | David Mycock |
| Correspondent | David Mycock IMMUNOSTICS, INC. 3505 SUNSET AVE. Ocean, NJ 07712 |
| Product Code | DHR |
| CFR Regulation Number | 866.5775 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1997-07-01 |
| Decision Date | 1997-11-25 |