FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
VITAJET
K Number: K962625
·
Decision Dec 10, 1996
Classifications
1
FEI Numbers
11
Registration Numbers
11
Same Product Code
52
Applicant Total
3
Review Days
158
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Basic Information
- Device Name
- VITAJET
- K Number
- K962625
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 880.5430
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Vitajet Corp.
- Date Received
- July 5, 1996
- Decision Date
- December 10, 1996
- Product Code
- KZE
- 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 |
|---|---|---|---|
| KZE | Injector, Fluid, Non-Electrically Powered | FDA class 2 | General Hospital |
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