Cleared Traditional

K002563 - SHEEP ANTI-HUMAN LAMBDA FREE LIGHT CHAIN IMMUNOFIXATION GRADE KIT (FDA 510(k) Clearance)

Oct 2000
Decision
70d
Days
Class 2
Risk

K002563 is an FDA 510(k) clearance for the SHEEP ANTI-HUMAN LAMBDA FREE LIGHT CHAIN IMMUNOFIXATION GRADE KIT. This device is classified as a Lambda, Antigen, Antiserum, Control (Class II - Special Controls, product code DEH).

Submitted by The Binding Site, Ltd. (Santa Monica, US). The FDA issued a Cleared decision on October 26, 2000, 70 days after receiving the submission on August 17, 2000.

This device falls under the Immunology FDA review panel. Regulated under 21 CFR 866.5550.

Submission Details

510(k) Number K002563 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 17, 2000
Decision Date October 26, 2000
Days to Decision 70 days
Submission Type Traditional
Review Panel Immunology (IM)
Summary Statement

Device Classification

Product Code DEH — Lambda, Antigen, Antiserum, Control
Device Class Class II - Special Controls
CFR Regulation 21 CFR 866.5550