The following data is part of a premarket notification filed by Immunotech, Inc. with the FDA for Opticlone Cd3/cd8 Monoclonal Antibodies.
Device ID | K952182 |
510k Number | K952182 |
Device Name: | OPTICLONE CD3/CD8 MONOCLONAL ANTIBODIES |
Classification | Counter, Differential Cell |
Applicant | IMMUNOTECH, INC. 160 B LARRABEE RD. Westbrook, ME 04092 |
Contact | James W Champlin |
Correspondent | James W Champlin IMMUNOTECH, INC. 160 B LARRABEE RD. Westbrook, ME 04092 |
Product Code | GKZ |
CFR Regulation Number | 864.5220 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1995-05-09 |
Decision Date | 1995-07-05 |