Human IgA liquid reagent kit for Use on SPAPlus
K-Number: K192116 · 2019-09-04
Device Summary
Frequently Asked Questions
What is the Human IgA liquid reagent kit for Use on SPAPlus?
Human IgA liquid reagent kit for Use on SPAPlus is a medical device that received FDA 510(k) clearance on 2019-09-04. It is manufactured by The Binding Site Group , Ltd.. The 510(k) number is K192116.
When was Human IgA liquid reagent kit for Use on SPAPlus approved by the FDA?
Human IgA liquid reagent kit for Use on SPAPlus received FDA 510(k) clearance on 2019-09-04, under approval number K192116.
What company makes Human IgA liquid reagent kit for Use on SPAPlus?
Human IgA liquid reagent kit for Use on SPAPlus is manufactured by The Binding Site Group , Ltd..
What is the FDA product code for Human IgA liquid reagent kit for Use on SPAPlus?
The FDA product code for Human IgA liquid reagent kit for Use on SPAPlus is CFN.
Related Clinical Trials
Other Devices by The Binding Site Group , Ltd.
Related Devices (Code: CFN)
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.