The following data is part of a premarket notification filed by Elias Usa, Inc. with the FDA for Elias Tmab.
| Device ID | K925923 |
| 510k Number | K925923 |
| Device Name: | ELIAS TMAB |
| Classification | System, Test, Thyroid Autoantibody |
| Applicant | ELIAS USA, INC. 373 280TH ST. Osceola, WI 54020 |
| Contact | Gottfried Kellermann |
| Correspondent | Gottfried Kellermann ELIAS USA, INC. 373 280TH ST. Osceola, WI 54020 |
| Product Code | JZO |
| CFR Regulation Number | 866.5870 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-11-23 |
| Decision Date | 1993-01-14 |