FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
ELITECH CLINICAL SYSTEMS CREATININE PAP SL, ELICAL 2, ELITROL I AND ELITROL II, URINE CONTROL BI-LEVEL
K Number: K132399
·
Decision Jan 3, 2014
Classifications
1
FEI Numbers
55
Registration Numbers
55
Same Product Code
48
Applicant Total
17
Review Days
155
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Basic Information
- Device Name
- ELITECH CLINICAL SYSTEMS CREATININE PAP SL, ELICAL 2, ELITROL I AND ELITROL II, URINE CONTROL BI-LEVEL
- K Number
- K132399
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 862.1225
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Elitechgroup
- Date Received
- August 1, 2013
- Decision Date
- January 3, 2014
- Product Code
- JFY
- 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 |
|---|---|---|---|
| JFY | Enzymatic Method, Creatinine | FDA class 2 | Clinical Chemistry |
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