FDA 510(k)
FDA class 2
Substantially Equivalent
🇰🇷 South Korea
QSCHECK UISACR
K Number: K252619
·
Decision Feb 20, 2026
Classifications
1
FEI Numbers
55
Registration Numbers
55
Same Product Code
48
Applicant Total
1
Review Days
185
Basic Information
- Device Name
- QSCHECK UISACR
- K Number
- K252619
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 862.1225
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Qstag, Inc.
- Date Received
- August 19, 2025
- Decision Date
- February 20, 2026
- Product Code
- JFY
- Advisory Committee
- Clinical Chemistry
- Review Advisory Committee
- CH
- 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 |
|---|---|---|---|
| JFY | Enzymatic Method, Creatinine | FDA class 2 | Clinical Chemistry |
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