FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
CX(TM) CANNABINOID 100 NG(THC) REAGENT/SYNCHRON CX SYS
K Number: K944088
·
Decision Nov 21, 1994
Classifications
1
FEI Numbers
103
Registration Numbers
103
Same Product Code
149
Applicant Total
281
Review Days
139
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Basic Information
- Device Name
- CX(TM) CANNABINOID 100 NG(THC) REAGENT/SYNCHRON CX SYS
- K Number
- K944088
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 862.3870
- Medical Specialty
- Clinical Toxicology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Beckman Instruments, Inc.
- Date Received
- July 5, 1994
- Decision Date
- November 21, 1994
- 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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