FDA 510(k)
FDA class 2
Substantially Equivalent
🇹🇼 Taiwan
U-RIGHT TD-4249/U-RIGHT TD-4250 BLOOD GLUCOSE MONITORING SYSTEM
K Number: K083570
·
Decision Mar 11, 2009
Classifications
1
FEI Numbers
131
Registration Numbers
131
Same Product Code
400
Applicant Total
123
Review Days
98
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Basic Information
- Device Name
- U-RIGHT TD-4249/U-RIGHT TD-4250 BLOOD GLUCOSE MONITORING SYSTEM
- K Number
- K083570
- Device Class
- FDA class 2
- Clearance Type
- Special
- Regulation Number
- 862.1345
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Taidoc Technology Corporation
- Date Received
- December 3, 2008
- Decision Date
- March 11, 2009
- Product Code
- CGA
- 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 |
|---|---|---|---|
| CGA | Glucose Oxidase, Glucose | FDA class 2 | Clinical Chemistry |
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