FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
CDT CYTOTOXI TEST
K Number: K883560
·
Decision Oct 25, 1988
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
41
Applicant Total
19
Review Days
67
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Basic Information
- Device Name
- CDT CYTOTOXI TEST
- K Number
- K883560
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 866.2660
- Medical Specialty
- Microbiology
- Decision
- Substantially Equivalent
- Applicant
- Advanced Clinical Diagnostics
- Date Received
- August 19, 1988
- Decision Date
- October 25, 1988
- Product Code
- LLH
- Advisory Committee
- Microbiology
- Review Advisory Committee
- MI
- 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 |
|---|---|---|---|
| LLH | Reagents, Clostridium Difficile Toxin | FDA class 1 | Microbiology |
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