FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
AVOXIMETER 4000
K Number: K951485
·
Decision Nov 6, 1995
Classifications
1
FEI Numbers
14
Registration Numbers
14
Same Product Code
7
Applicant Total
3
Review Days
221
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Basic Information
- Device Name
- AVOXIMETER 4000
- K Number
- K951485
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 862.3220
- Medical Specialty
- Clinical Toxicology
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- A-Vox Systems, Inc.
- Date Received
- March 30, 1995
- Decision Date
- November 6, 1995
- Product Code
- JKS
- Advisory Committee
- Clinical Toxicology
- Review Advisory Committee
- TX
- 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 |
|---|---|---|---|
| JKS | Spectral Absorb. Curve, Oxyhemoglobin, Carboxyhemoglobin, Carbon-Monoxide | FDA class 1 | Clinical Toxicology |
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