LASERBRUSH— 510(k) K121920
Substantially EquivalentSunetics International Marketing Group, LLC
FDA 510(k) clearance K121920 for LASERBRUSH, Substantially Equivalent on 2013-06-27. Applicant: Sunetics International Marketing Group, LLC. Device class: 2.
Clearance details
- Applicant
- Sunetics International Marketing Group, LLC
- Product code
- Code OAP
- Device class
- Class 2
- Regulation
- 21 CFR 890.5500
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Rockwall, TX, US
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