FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
BELIMED STEAM STERILIZER MST-V
K Number: K130172
·
Decision Sep 23, 2013
Classifications
1
FEI Numbers
57
Registration Numbers
57
Same Product Code
179
Applicant Total
1
Review Days
242
Basic Information
- Device Name
- BELIMED STEAM STERILIZER MST-V
- K Number
- K130172
- Device Class
- FDA class 2
- Clearance Type
- Abbreviated
- Regulation Number
- 880.6880
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- BELIMED, INC.
- Date Received
- January 24, 2013
- Decision Date
- September 23, 2013
- Product Code
- FLE
- 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 |
|---|---|---|---|
| FLE | Sterilizer, Steam | FDA class 2 | General Hospital |
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