The following data is part of a premarket notification filed by Immuno Assay Corp. with the FDA for Tbg Diagnostic Kit.
| Device ID | K811725 |
| 510k Number | K811725 |
| Device Name: | TBG DIAGNOSTIC KIT |
| Classification | Electrophoretic, Protein Fractionation |
| Applicant | IMMUNO ASSAY CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | CEF |
| CFR Regulation Number | 862.1630 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-06-18 |
| Decision Date | 1981-07-10 |