510(k) K952789

OPTICLONE CD4FITC/CD8 PE MONOCLONAL ANTIBODIES by Immunotech Corp. — Product Code GKZ

K952789 is an FDA 510(k) premarket notification submitted by Immunotech Corp. for the device "OPTICLONE CD4FITC/CD8 PE MONOCLONAL ANTIBODIES". The FDA issued a decision of Substantially Equivalent on August 14, 1995. The device falls under product code GKZ (Counter, Differential Cell), a Class II device regulated under 21 CFR 864.5220. Immunotech Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 14, 1995
Date Received
June 19, 1995
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Counter, Differential Cell
Device Class
Class II
Regulation Number
864.5220
Review Panel
HE
Submission Type