The following data is part of a premarket notification filed by Abbott Laboratories with the FDA for Cell-dyn 4000 Immuno T-cell (cd3/4/8) Assay.
Device ID | K010953 |
510k Number | K010953 |
Device Name: | CELL-DYN 4000 IMMUNO T-CELL (CD3/4/8) ASSAY |
Classification | Counter, Differential Cell |
Applicant | ABBOTT LABORATORIES 5440 PATRICK HENRY DR. Santa Clara, CA 95054 |
Contact | John Dean |
Correspondent | John Dean ABBOTT LABORATORIES 5440 PATRICK HENRY DR. Santa Clara, CA 95054 |
Product Code | GKZ |
CFR Regulation Number | 864.5220 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2001-03-30 |
Decision Date | 2001-06-06 |