The following data is part of a premarket notification filed by Immco Diagnostics, Inc. with the FDA for Immulisa Anti-human Tissue Transglutaminase (hu-ttg) Antibody Iga Elisa.
Device ID | K032571 |
510k Number | K032571 |
Device Name: | IMMULISA ANTI-HUMAN TISSUE TRANSGLUTAMINASE (HU-TTG) ANTIBODY IGA ELISA |
Classification | Autoantibodies, Endomysial(tissue Transglutaminase) |
Applicant | IMMCO DIAGNOSTICS, INC. 60 PINEVIEW DR. Buffalo, NY 14228 |
Contact | Kevin Lawson |
Correspondent | Kevin Lawson IMMCO DIAGNOSTICS, INC. 60 PINEVIEW DR. Buffalo, NY 14228 |
Product Code | MVM |
CFR Regulation Number | 866.5660 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2003-08-20 |
Decision Date | 2003-12-24 |