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FDA 510(k)

Human IgA liquid reagent kit for Use on SPAPlus

K-Number: K192116 · 2019-09-04

Decision Date2019-09-04
Product CodeCFN
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

Human IgA liquid reagent kit for Use on SPAPlus is a medical device manufactured by The Binding Site Group , Ltd.. It received FDA 510(k) clearance on 2019-09-04 under approval number K192116. The device is classified under product code CFN. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

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.

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Official Source

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