The following data is part of a premarket notification filed by London Diagnostics, Inc. with the FDA for Lumatag Free T4 Chemiluminescence Assay.
Device ID | K914835 |
510k Number | K914835 |
Device Name: | LUMATAG FREE T4 CHEMILUMINESCENCE ASSAY |
Classification | Radioimmunoassay, Free Thyroxine |
Applicant | LONDON DIAGNOSTICS, INC. 10300 VALLEY VIEW RD. SUITE 107 Eden Prairie, MN 55344 |
Contact | K Ramakrishnan |
Correspondent | K Ramakrishnan LONDON DIAGNOSTICS, INC. 10300 VALLEY VIEW RD. SUITE 107 Eden Prairie, MN 55344 |
Product Code | CEC |
CFR Regulation Number | 862.1695 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1991-10-25 |
Decision Date | 1991-12-17 |