PurGuard360(QF10)

FDA 510(k) K261470 · E.A.M Benelux B.V

Substantially Equivalent

510(k) numberK261470

Submission

Device name
PurGuard360(QF10)
Applicant
E.A.M Benelux B.V
Almere, NL
Received
May 4, 2026
Decision date
September 9, 2026
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
NHV – System, Water Purification, General Medical Use
Device class
Class II (moderate risk)
Regulation
21 CFR 876.5665
Specialty
Gastroenterology, Urology

The device is a portable water treatment system which features components and technology similar to water treatment systems previously cleared for hemodialysis. The difference lies with the intended use, as the proposed device is not intended for use in hemodialysis applications, for which a product code currently exists. Instead, the proposed device is intended for use to purify water for…

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Questions and answers

When was PurGuard360(QF10) cleared by the FDA?

PurGuard360(QF10) (K261470) received a 510(k) decision of Substantially Equivalent on September 9, 2026, 128 days after the submission was received.

What is the product code of K261470?

The FDA product code is NHV – System, Water Purification, General Medical Use, a Class II (moderate risk) device regulated under 21 CFR 876.5665.