FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
KLORMAN
K Number: K923693
·
Decision Jan 23, 1996
Classifications
1
FEI Numbers
386
Registration Numbers
386
Same Product Code
72
Applicant Total
14
Review Days
1279
Basic Information
- Device Name
- KLORMAN
- K Number
- K923693
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 880.6890
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- MATRIX MEDICA, INC.
- Date Received
- July 23, 1992
- Decision Date
- January 23, 1996
- Product Code
- LRJ
- Advisory Committee
- General Hospital
- Review Advisory Committee
- HO
- 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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