FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
GLOOKO DEVICE SYSTEM FOR GLOOKO APPLICATION
K Number: K132272
·
Decision Oct 17, 2013
Classifications
1
FEI Numbers
177
Registration Numbers
178
Same Product Code
506
Applicant Total
3
Review Days
87
Basic Information
- Device Name
- GLOOKO DEVICE SYSTEM FOR GLOOKO APPLICATION
- K Number
- K132272
- Device Class
- FDA class 2
- Clearance Type
- Special
- Regulation Number
- 862.1345
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- GLOOKO, INC.
- Date Received
- July 22, 2013
- Decision Date
- October 17, 2013
- 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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