FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
ALCO-BREATH TUBE, CHECKPOINT BREATH ALCOHOL TEST
K Number: K102225
·
Decision Apr 6, 2011
Classifications
1
FEI Numbers
41
Registration Numbers
41
Same Product Code
27
Applicant Total
1
Review Days
240
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Basic Information
- Device Name
- ALCO-BREATH TUBE, CHECKPOINT BREATH ALCOHOL TEST
- K Number
- K102225
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 862.3050
- Medical Specialty
- Clinical Toxicology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Alcopro, Inc.
- Date Received
- August 9, 2010
- Decision Date
- April 6, 2011
- 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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