The following data is part of a premarket notification filed by Immuno Assay Corp. with the FDA for T4 Ria Kit.
Device ID | K810811 |
510k Number | K810811 |
Device Name: | T4 RIA KIT |
Classification | Radioimmunoassay, Total Thyroxine |
Applicant | IMMUNO ASSAY CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | CDX |
CFR Regulation Number | 862.1700 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1981-03-24 |
Decision Date | 1981-04-07 |