FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
ALCOMATE, MODEL CA2000
K Number: K041334
·
Decision Aug 11, 2004
Classifications
1
FEI Numbers
41
Registration Numbers
41
Same Product Code
27
Applicant Total
4
Review Days
84
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Basic Information
- Device Name
- ALCOMATE, MODEL CA2000
- K Number
- K041334
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 862.3050
- Medical Specialty
- Clinical Toxicology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Khn Solutions, LLC
- Date Received
- May 19, 2004
- Decision Date
- August 11, 2004
- Product Code
- DJZ
- 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 |
|---|---|---|---|
| DJZ | Devices, Breath Trapping, Alcohol | FDA class 1 | Clinical Toxicology |
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