FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
TRIOS SYSTEM
K Number: K090399
·
Decision Jun 10, 2009
Classifications
1
FEI Numbers
92
Registration Numbers
93
Same Product Code
73
Applicant Total
11
Review Days
113
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Basic Information
- Device Name
- TRIOS SYSTEM
- K Number
- K090399
- 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
- Viora , Ltd.
- Date Received
- February 17, 2009
- Decision Date
- June 10, 2009
- Product Code
- ONF
- 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 |
|---|---|---|---|
| ONF | Powered Light Based Non-Laser Surgical Instrument With Thermal Effect | FDA class 2 | General, Plastic Surgery |
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Other Clearances by Viora , Ltd.
| K Number | Device Name | ||
|---|---|---|---|
| K202247 | V30 system, V20 system, V10 system, V-VR Hand piece | Dec 9, 2020 | Substantially Equivalent |
| K201064 | V30 System, V20 System, V10 System, V-FR Handpiece | Jul 15, 2020 | Substantially Equivalent |
| K200468 | V30 system, V20 system, V10 system, V-FC Handpiece | May 21, 2020 | Substantially Equivalent |
| K162363 | V30 system, V-Form Handpiece BC Medium applicator | Nov 18, 2016 | Substantially Equivalent |
| K152611 | V20 system | Feb 19, 2016 | Substantially Equivalent |
| K150035 | V10 system | May 1, 2015 | Substantially Equivalent |
| K142093 | V20 SYSTEM | Nov 14, 2014 | Substantially Equivalent |
| K141904 | VIORA V-TOUCH | Oct 21, 2014 | Substantially Equivalent |
| K133837 | VIORA V-TOTAL | Apr 9, 2014 | Substantially Equivalent |
| K090221 | REACTION SYSTEM | Jul 1, 2009 | Substantially Equivalent |