FDA 510(k)
FDA class 2
Substantially Equivalent
🇨🇭 Switzerland
MEDELA DOMINANT 50 LIPO, MODEL 600-5706
K Number: K063336
·
Decision Feb 26, 2007
Classifications
1
FEI Numbers
48
Registration Numbers
48
Same Product Code
57
Applicant Total
30
Review Days
112
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Basic Information
- Device Name
- MEDELA DOMINANT 50 LIPO, MODEL 600-5706
- K Number
- K063336
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 878.5040
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Medela AG
- Date Received
- November 6, 2006
- Decision Date
- February 26, 2007
- Product Code
- QPB
- Advisory Committee
- General, Plastic Surgery
- Review Advisory Committee
- SU
- 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 |
|---|---|---|---|
| QPB | System, Suction, Lipoplasty For Removal | FDA class 2 | General, Plastic Surgery |
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