FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
ARTERIA BLOOD FILTER
K Number: K021293
·
Decision Aug 22, 2002
Classifications
1
FEI Numbers
50
Registration Numbers
50
Same Product Code
97
Applicant Total
3
Review Days
121
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Basic Information
- Device Name
- ARTERIA BLOOD FILTER
- K Number
- K021293
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 880.5440
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Arteria Medical Science, Inc.
- Date Received
- April 23, 2002
- Decision Date
- August 22, 2002
- Product Code
- FPB
- Advisory Committee
- General Hospital
- Review Advisory Committee
- HO
- 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 |
|---|---|---|---|
| FPB | Filter, Infusion Line | FDA class 2 | General Hospital |
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