FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
LABELING SUBMITTAL, ADX AMPHETAMINE/METHAMPHETA.II
K Number: K895210
·
Decision Sep 25, 1989
Classifications
1
FEI Numbers
96
Registration Numbers
96
Same Product Code
224
Applicant Total
883
Review Days
38
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Basic Information
- Device Name
- LABELING SUBMITTAL, ADX AMPHETAMINE/METHAMPHETA.II
- K Number
- K895210
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 862.3100
- Medical Specialty
- Clinical Toxicology
- Decision
- Substantially Equivalent
- Applicant
- Abbott Laboratories
- Date Received
- August 18, 1989
- Decision Date
- September 25, 1989
- Product Code
- DKZ
- 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 |
|---|---|---|---|
| DKZ | Enzyme Immunoassay, Amphetamine | FDA class 2 | Clinical Toxicology |
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