FDA 510(k)
FDA class 2
Substantially Equivalent
🇨🇦 Canada
ACETAMINOPHEN ASSAY
K Number: K952949
·
Decision Sep 6, 1995
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
35
Applicant Total
66
Review Days
72
Basic Information
- Device Name
- ACETAMINOPHEN ASSAY
- K Number
- K952949
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 862.3030
- Medical Specialty
- Clinical Toxicology
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- DIAGNOSTIC CHEMICALS LTD.
- Date Received
- June 26, 1995
- Decision Date
- September 6, 1995
- Product Code
- LDP
- 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 |
|---|---|---|---|
| LDP | Colorimetry, Acetaminophen | FDA class 2 | Clinical Toxicology |
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