FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
VISION CREATININE
K Number: K854846
·
Decision Jan 13, 1986
Classifications
1
FEI Numbers
39
Registration Numbers
39
Same Product Code
158
Applicant Total
883
Review Days
40
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Basic Information
- Device Name
- VISION CREATININE
- K Number
- K854846
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 862.1225
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Applicant
- Abbott Laboratories
- Date Received
- December 4, 1985
- Decision Date
- January 13, 1986
- Product Code
- CGX
- 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 |
|---|---|---|---|
| CGX | Alkaline Picrate, Colorimetry, Creatinine | FDA class 2 | Clinical Chemistry |
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