The following data is part of a premarket notification filed by Thyroid Diagnostics, Inc. with the FDA for J & S Iron Saturating Reagent.
| Device ID | K811942 |
| 510k Number | K811942 |
| Device Name: | J & S IRON SATURATING REAGENT |
| Classification | Bathophenanthroline, Iron Binding Capacity |
| Applicant | THYROID DIAGNOSTICS, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | JQF |
| CFR Regulation Number | 862.1415 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-07-07 |
| Decision Date | 1981-09-08 |