FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
R&D RET-LINE KIT
K Number: K013898
·
Decision Jan 22, 2002
Classifications
1
FEI Numbers
32
Registration Numbers
32
Same Product Code
191
Applicant Total
79
Review Days
60
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Basic Information
- Device Name
- R&D RET-LINE KIT
- K Number
- K013898
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 864.8625
- Medical Specialty
- Hematology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- R&D Systems, Inc.
- Date Received
- November 23, 2001
- Decision Date
- January 22, 2002
- Product Code
- JPK
- Advisory Committee
- Hematology
- Review Advisory Committee
- HE
- 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 |
|---|---|---|---|
| JPK | Mixture, Hematology Quality Control | FDA class 2 | Hematology |
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