VELASMOOTH, SHAPER
FDA 510(k) clearance K050397 · decided 2005-06-09
Clearance details
- K-number
- K050397
- Device name
- VELASMOOTH, SHAPER
- Applicant
- Syneron Medical, Ltd.
- Decision
- Substantially Equivalent
- Date received
- 2005-02-16
- Decision date
- 2005-06-09
- Days to decision
- 113 days
- Clearance type
- Traditional
- Product code
- NUV
- Device class
- 2
- Regulation number
- 878.4810
- Medical specialty
- General, Plastic Surgery
- Advisory committee
- General, Plastic Surgery
- Location
- Washington, DC, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.