FDA 510(k) FDA class 2 Substantially Equivalent 🇲🇽 Mexico

NIKKICART

K Number: K221652 · Decision Mar 3, 2023
Classifications
1
FEI Numbers
35
Registration Numbers
35
Same Product Code
122
Applicant Total
1
Review Days
269

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Basic Information

Device Name
NIKKICART
K Number
K221652
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5820
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Renal Care Dialysis Solutions, S.A. DE C.V.
Date Received
June 7, 2022
Decision Date
March 3, 2023
Product Code
KPO
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
KPO Dialysate Concentrate For Hemodialysis (Liquid Or Powder)

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