FDA 510(k)
FDA class 2
Substantially Equivalent
🇨🇳 China
VivaChek Link Plus Blood Glucose Monitoring System
K Number: K233058
·
Decision Dec 22, 2023
Classifications
1
FEI Numbers
168
Registration Numbers
169
Same Product Code
507
Applicant Total
10
Review Days
88
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Basic Information
- Device Name
- VivaChek Link Plus Blood Glucose Monitoring System
- K Number
- K233058
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 862.1345
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Vivachek Biotech (Hangzhou) Co., Ltd.
- Date Received
- September 25, 2023
- Decision Date
- December 22, 2023
- Product Code
- NBW
- 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 |
|---|---|---|---|
| NBW | System, Test, Blood Glucose, Over The Counter | FDA class 2 | Clinical Chemistry |
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| K192957 | VivaChek Blood Glucose and B-Ketone Monitoring System | Jun 5, 2020 | Substantially Equivalent |