PDF — Immunoglobulin M Lambda Heavy And Light Chain Combined Class II

FDA Device Classification

FDA product code PDF covers "Immunoglobulin M Lambda Heavy And Light Chain Combined", a Class II medical device regulated under 21 CFR 866.5510. Submissions are reviewed by the Immunology panel.

Classification Details

Product Code
PDF
Device Class
Class II
Regulation Number
866.5510
Submission Type
Review Panel
IM
Medical Specialty
Immunology
Implant
No

Definition

Intended for the in-vitro quantification of IgM lambda concentration in human serum. The result is to be used with previously diagnosed IgM Waldenstoms Macrolobulinaemia, in conjunction with other clinical and laboratory findings.