510(k) K231290

Optilite® Freelite® Kappa Free Kit, Optilite® Freelite® Lambda Free Kit by The Binding Site, Ltd. — Product Code DFH

K231290 is an FDA 510(k) premarket notification submitted by The Binding Site, Ltd. for the device "Optilite® Freelite® Kappa Free Kit, Optilite® Freelite® Lambda Free Kit". The FDA issued a decision of Substantially Equivalent on January 24, 2024. The device falls under product code DFH (Kappa, Antigen, Antiserum, Control), a Class II device regulated under 21 CFR 866.5550. The Binding Site, Ltd. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 24, 2024
Date Received
May 4, 2023
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Kappa, Antigen, Antiserum, Control
Device Class
Class II
Regulation Number
866.5550
Review Panel
IM
Submission Type