The following data is part of a premarket notification filed by Calbiochem-behring Corp. with the FDA for Triiodothyronine Radioimmun. System.
Device ID | K801123 |
510k Number | K801123 |
Device Name: | TRIIODOTHYRONINE RADIOIMMUN. SYSTEM |
Classification | Radioimmunoassay, Total Triiodothyronine |
Applicant | CALBIOCHEM-BEHRING CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | CDP |
CFR Regulation Number | 862.1710 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1980-05-12 |
Decision Date | 1980-06-09 |