FDA 510(k)
FDA class 2
Substantially Equivalent
🇨🇳 China
Diosculpt
K Number: K222265
·
Decision Sep 23, 2022
Classifications
1
FEI Numbers
16
Registration Numbers
16
Same Product Code
18
Applicant Total
6
Review Days
57
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Basic Information
- Device Name
- Diosculpt
- K Number
- K222265
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 878.5400
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Shanghai Wonderful Opto-Electrics Tech.Co.,Ltd
- Date Received
- July 28, 2022
- Decision Date
- September 23, 2022
- Product Code
- PKT
- 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 |
|---|---|---|---|
| PKT | Laser For Disruption Of Adipocyte Cells For Aesthetic Use | FDA class 2 | General, Plastic Surgery |
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