FDA 510(k)
FDA class 2
Unknown
🇺🇸 United States
VIA 1-01 INFUSION PUMP/BLOOD CHEM. SYST. -- MOD.
K Number: K922997
·
Decision Jan 11, 1994
Classifications
1
FEI Numbers
2
Registration Numbers
2
Same Product Code
6
Applicant Total
4
Review Days
568
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Basic Information
- Device Name
- VIA 1-01 INFUSION PUMP/BLOOD CHEM. SYST. -- MOD.
- K Number
- K922997
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 880.5725
- Medical Specialty
- General Hospital
- Decision
- Unknown
- Statement or Summary
- Statement
- Applicant
- Via Medical Corp.
- Date Received
- June 22, 1992
- Decision Date
- January 11, 1994
- Product Code
- LZF
- 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 |
|---|---|---|---|
| LZF | Pump, Infusion, Analytical Sampling | FDA class 2 | General Hospital |
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