The following data is part of a premarket notification filed by Cytotech, Inc. with the FDA for Circulating Immune Complexes Controls.
Device ID | K882829 |
510k Number | K882829 |
Device Name: | CIRCULATING IMMUNE COMPLEXES CONTROLS |
Classification | Complement C1q, Antigen, Antiserum, Control |
Applicant | CYTOTECH, INC. 11035 ROSELLE STREET, SUITE A San Diego, CA 92121 |
Contact | John D Tamerius |
Correspondent | John D Tamerius CYTOTECH, INC. 11035 ROSELLE STREET, SUITE A San Diego, CA 92121 |
Product Code | DAK |
CFR Regulation Number | 866.5240 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1988-07-08 |
Decision Date | 1988-08-04 |