FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

ELISIO™-H

K Number: K260533 · Decision Mar 19, 2026
Classifications
1
FEI Numbers
89
Registration Numbers
89
Same Product Code
343
Applicant Total
34
Review Days
30

Basic Information

Device Name
ELISIO™-H
K Number
K260533
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
876.5860
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Nipro Medical Corporation
Date Received
February 17, 2026
Decision Date
March 19, 2026
Product Code
KDI
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System

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