The following data is part of a premarket notification filed by Coulter Immunology with the FDA for Coulter Clone T8 Monoclonal Antibody.
| Device ID | K893853 |
| 510k Number | K893853 |
| Device Name: | COULTER CLONE T8 MONOCLONAL ANTIBODY |
| Classification | Counter, Differential Cell |
| Applicant | COULTER IMMUNOLOGY 440 COULTER WAY WEST 20TH STREET Hialeah, FL 33010 |
| Contact | Gregory Butchko |
| Correspondent | Gregory Butchko COULTER IMMUNOLOGY 440 COULTER WAY WEST 20TH STREET Hialeah, FL 33010 |
| Product Code | GKZ |
| CFR Regulation Number | 864.5220 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1989-05-25 |
| Decision Date | 1990-03-02 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 15099590542368 | K893853 | 000 |
| 15099590540227 | K893853 | 000 |
| 15099590539610 | K893853 | 000 |
| 15099590537012 | K893853 | 000 |