FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
25-OH VITAMIN D ELISA
K Number: K123660
·
Decision Jul 17, 2013
Classifications
1
FEI Numbers
51
Registration Numbers
51
Same Product Code
45
Applicant Total
12
Review Days
231
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Basic Information
- Device Name
- 25-OH VITAMIN D ELISA
- K Number
- K123660
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 862.1825
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Euroimmun US
- Date Received
- November 28, 2012
- Decision Date
- July 17, 2013
- Product Code
- MRG
- 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 |
|---|---|---|---|
| MRG | System, Test, Vitamin D | FDA class 2 | Clinical Chemistry |
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