FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
LIBERTY NORMAL GLUCOSE CONTROL SOLUTION
K Number: K060706
·
Decision Apr 28, 2006
Classifications
1
FEI Numbers
269
Registration Numbers
269
Same Product Code
492
Applicant Total
5
Review Days
43
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Basic Information
- Device Name
- LIBERTY NORMAL GLUCOSE CONTROL SOLUTION
- K Number
- K060706
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 862.1660
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Liberty Healthcare Group, Inc.
- Date Received
- March 16, 2006
- Decision Date
- April 28, 2006
- Product Code
- JJX
- 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 |
|---|---|---|---|
| JJX | Single (Specified) Analyte Controls (Assayed And Unassayed) | FDA class 1 | Clinical Chemistry |
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Other Clearances by Liberty Healthcare Group, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K063855 | LIBERTY NORMAL GLUCOSE CONTROL SOLUTION, MODEL 2120045/ HIGH GLUCOSE CONTROL SOLUTION, MODEL 2120047 | Feb 1, 2007 | Substantially Equivalent |
| K060481 | LIBERTY GLUCOSE CONTROL SOLUTION | Mar 9, 2006 | Substantially Equivalent |
| K060426 | LIBERTY GLUCOSE NORMAL CONTROL SOLUTIONS, MODEL 2120041 | Mar 9, 2006 | Substantially Equivalent |
| K052980 | LIBERTY GLUCOSE CONTROL, MODEL 2120031 | Nov 30, 2005 | Substantially Equivalent |