Pall QPoint Water Filter Capsule (Shower), Pall QPoint Water Filter Capsule (Faucet)

FDA 510(k) K163609 · Pall International Sarl

Substantially Equivalent

510(k) numberK163609

Submission

Device name
Pall QPoint Water Filter Capsule (Shower), Pall QPoint Water Filter Capsule (Faucet)
Applicant
Pall International Sarl
Fribourg, CH
Received
December 22, 2016
Decision date
June 1, 2017
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 Pall QPoint Water Filter Capsule (Shower), Pall QPoint Water Filter Capsule (Faucet) cleared by the FDA?

Pall QPoint Water Filter Capsule (Shower), Pall QPoint Water Filter Capsule (Faucet) (K163609) received a 510(k) decision of Substantially Equivalent on June 1, 2017, 161 days after the submission was received.

What is the product code of K163609?

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