FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
EXSPOR
K Number: K953241
·
Decision Sep 29, 1995
Classifications
1
FEI Numbers
370
Registration Numbers
370
Same Product Code
72
Applicant Total
4
Review Days
80
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Basic Information
- Device Name
- EXSPOR
- K Number
- K953241
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 880.6890
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Alcide Corp.
- Date Received
- July 11, 1995
- Decision Date
- September 29, 1995
- Product Code
- LRJ
- Advisory Committee
- General Hospital
- Review Advisory Committee
- GU
- 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 |
|---|---|---|---|
| LRJ | Disinfectant, Medical Devices | FDA class 1 | General Hospital |
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