FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
REVISED LABELING FOR ADX CANNABINOIDS
K Number: K880015
·
Decision Mar 1, 1988
Classifications
1
FEI Numbers
103
Registration Numbers
103
Same Product Code
149
Applicant Total
883
Review Days
57
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Basic Information
- Device Name
- REVISED LABELING FOR ADX CANNABINOIDS
- K Number
- K880015
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 862.3870
- Medical Specialty
- Clinical Toxicology
- Decision
- Substantially Equivalent
- Applicant
- Abbott Laboratories
- Date Received
- January 4, 1988
- Decision Date
- March 1, 1988
- Product Code
- LDJ
- 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 |
|---|---|---|---|
| LDJ | Enzyme Immunoassay, Cannabinoids | FDA class 2 | Clinical Toxicology |
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