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SkinPen Precision System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
DEN160029
510(k) Type
Direct
Applicant
BELLUS MEDICAL, LLC.
Country
United States
FDA Decision
Deleted
Decision Date
3/1/2018
Days to Decision
604 days

SkinPen Precision System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
DEN160029
510(k) Type
Direct
Applicant
BELLUS MEDICAL, LLC.
Country
United States
FDA Decision
Deleted
Decision Date
3/1/2018
Days to Decision
604 days