FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
ACCELAWAVE SYSTEM
K Number: K082484
·
Decision Sep 12, 2008
Classifications
1
FEI Numbers
97
Registration Numbers
98
Same Product Code
70
Applicant Total
3
Review Days
15
Basic Information
- Device Name
- ACCELAWAVE SYSTEM
- K Number
- K082484
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 878.4810
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- GENESIS BIOSYSTEMS, INC.
- Date Received
- August 28, 2008
- Decision Date
- September 12, 2008
- Product Code
- ONF
- Advisory Committee
- General, Plastic Surgery
- Review Advisory Committee
- SU
- Third Party
- Y
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| ONF | Powered Light Based Non-Laser Surgical Instrument With Thermal Effect | FDA class 2 | General, Plastic Surgery |
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