Diazyme Human Kappa Free Light Chain Assay; Diazyme Human Lambda Free Light Chain Assay
K-Number: K181438 · 2018-06-26
Device Summary
Frequently Asked Questions
What is the Diazyme Human Kappa Free Light Chain Assay; Diazyme Human Lambda Free Light Chain Assay?
Diazyme Human Kappa Free Light Chain Assay; Diazyme Human Lambda Free Light Chain Assay is a medical device that received FDA 510(k) clearance on 2018-06-26. It is manufactured by Diazyme Laboratories, Inc.. The 510(k) number is K181438.
When was Diazyme Human Kappa Free Light Chain Assay; Diazyme Human Lambda Free Light Chain Assay approved by the FDA?
Diazyme Human Kappa Free Light Chain Assay; Diazyme Human Lambda Free Light Chain Assay received FDA 510(k) clearance on 2018-06-26, under approval number K181438.
What company makes Diazyme Human Kappa Free Light Chain Assay; Diazyme Human Lambda Free Light Chain Assay?
Diazyme Human Kappa Free Light Chain Assay; Diazyme Human Lambda Free Light Chain Assay is manufactured by Diazyme Laboratories, Inc..
What is the FDA product code for Diazyme Human Kappa Free Light Chain Assay; Diazyme Human Lambda Free Light Chain Assay?
The FDA product code for Diazyme Human Kappa Free Light Chain Assay; Diazyme Human Lambda Free Light Chain Assay is DFH.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.