NUBRILLIANCE PULSED LIGHT HAIR REMOVAL DEVICE— 510(k) K132518
Substantially EquivalentWellquest Intl., Inc.
FDA 510(k) clearance K132518 for NUBRILLIANCE PULSED LIGHT HAIR REMOVAL DEVICE, Substantially Equivalent on 2014-08-17. Applicant: Wellquest Intl., Inc..
Clearance details
- Applicant
- Wellquest Intl., Inc.
- Product code
- Code OHT
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Austin, TX, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.