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 | Device Class | Medical Specialty |
|---|---|---|---|
| KPO | Dialysate Concentrate For Hemodialysis (Liquid Or Powder) | FDA class 2 | Gastroenterology, Urology |
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