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NUBRILLIANCE PULSED LIGHT HAIR REMOVAL DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K132518
510(k) Type
Traditional
Applicant
WELLQUEST INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/17/2014
Days to Decision
370 days
Submission Type
Summary

NUBRILLIANCE PULSED LIGHT HAIR REMOVAL DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K132518
510(k) Type
Traditional
Applicant
WELLQUEST INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/17/2014
Days to Decision
370 days
Submission Type
Summary