510(k) K222727

Device
i3 ONE (203100-S);i3 TWO connect (203200-S);i3 TWO direct (203300-S)
Applicant
I3 Membrane GmbH
510(k) number
K222727
Product code
NHV
Decision
Substantially Equivalent (SESE)
Decision date
2023-06-02
Date received
2022-09-08
Regulation
876.5665
Classification name
System, Water Purification, General Medical Use
Medical specialty
Gastroenterology, Urology
Review panel
Gastroenterology, Urology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
Stephan Brinke-Seiferth
Address
Christoph-Seydel-Strasse 1 Radeberg DE 01454 01454

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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