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

CleanCart A, CleanCart C, AK 98 Hemodialysis Machine

K Number: K232467 · Decision Sep 14, 2023
Classifications
1
FEI Numbers
89
Registration Numbers
89
Same Product Code
343
Applicant Total
61
Review Days
30

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Basic Information

Device Name
CleanCart A, CleanCart C, AK 98 Hemodialysis Machine
K Number
K232467
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
876.5860
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Baxter Healthcare Corporation
Date Received
August 15, 2023
Decision Date
September 14, 2023
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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