FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
VITALMIX PLUS EMPTY I.V. CONTAINER
K Number: K972464
·
Decision Nov 5, 1997
Classifications
1
FEI Numbers
86
Registration Numbers
86
Same Product Code
116
Applicant Total
5
Review Days
127
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Basic Information
- Device Name
- VITALMIX PLUS EMPTY I.V. CONTAINER
- K Number
- K972464
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 880.5025
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Pacific Device, Inc.
- Date Received
- July 1, 1997
- Decision Date
- November 5, 1997
- Product Code
- KPE
- 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 |
|---|---|---|---|
| KPE | Container, I.V. | FDA class 2 | General Hospital |
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