The following data is part of a premarket notification filed by Cronus with the FDA for I-125 Anti-thyroglobulin Antibody Irma Test Kit.
Device ID | K871193 |
510k Number | K871193 |
Device Name: | I-125 ANTI-THYROGLOBULIN ANTIBODY IRMA TEST KIT |
Classification | System, Test, Thyroid Autoantibody |
Applicant | CRONUS P.O. BOX 1827 Carlsbad, CA 92008 |
Contact | Bob Cowden |
Correspondent | Bob Cowden CRONUS P.O. BOX 1827 Carlsbad, CA 92008 |
Product Code | JZO |
CFR Regulation Number | 866.5870 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1987-03-24 |
Decision Date | 1987-05-15 |