The following data is part of a premarket notification filed by American Diagnostic Corp. with the FDA for T3 Uptake Test System.
| Device ID | K802468 |
| 510k Number | K802468 |
| Device Name: | T3 UPTAKE TEST SYSTEM |
| Classification | Radioassay, Triiodothyronine Uptake |
| Applicant | AMERICAN DIAGNOSTIC CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KHQ |
| CFR Regulation Number | 862.1715 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1980-10-09 |
| Decision Date | 1980-10-31 |