FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
ADVIA CHEMISTRY MICROALBUMIN CALIBRATORS, _2 CALIBRATORS
K Number: K072204
·
Decision Oct 5, 2007
Classifications
1
FEI Numbers
101
Registration Numbers
101
Same Product Code
301
Applicant Total
11
Review Days
58
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Basic Information
- Device Name
- ADVIA CHEMISTRY MICROALBUMIN CALIBRATORS, _2 CALIBRATORS
- K Number
- K072204
- Device Class
- FDA class 2
- Clearance Type
- Abbreviated
- Regulation Number
- 862.1150
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Siemens Medical Solutions Diagnostics
- Date Received
- August 8, 2007
- Decision Date
- October 5, 2007
- Product Code
- JIX
- 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 |
|---|---|---|---|
| JIX | Calibrator, Multi-Analyte Mixture | FDA class 2 | Clinical Chemistry |
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|---|---|---|---|
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| K072794 | IMMULITE 2500 OM-MA, MODEL L5KOP | Nov 5, 2007 | Substantially Equivalent |
| K071466 | DCA VANTAGE, MODEL 5075 | Oct 9, 2007 | Substantially Equivalent |
| K070727 | ADVIA CHEMISTRY ENZYMATIC CREATININE_2 | Aug 3, 2007 | Substantially Equivalent |
| K071017 | IMMULITE 2500 HIGH SENSITIVITY C-REACTIVE PROTEIN, MODELS L5KCRP (200 TESTS), L5KCRP (600 TESTS) | May 2, 2007 | Substantially Equivalent |