FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
CoolSculpting System
K Number: K172144
·
Decision Nov 1, 2017
Classifications
1
FEI Numbers
19
Registration Numbers
19
Same Product Code
13
Applicant Total
4
Review Days
107
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Basic Information
- Device Name
- CoolSculpting System
- K Number
- K172144
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 878.4340
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Zeltiq Aesthetics
- Date Received
- July 17, 2017
- Decision Date
- November 1, 2017
- Product Code
- OOK
- 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 |
|---|---|---|---|
| OOK | Dermal Cooling Pack/Vacuum/Massager | FDA class 2 | General, Plastic Surgery |
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