Last synced on 25 January 2026 at 3:41 am

SOPIX INSIDE, SOPIX2 INSIDE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K140013
510(k) Type
Traditional
Applicant
Sopro - Acteon Group
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/5/2014
Days to Decision
246 days
Submission Type
Statement

SOPIX INSIDE, SOPIX2 INSIDE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K140013
510(k) Type
Traditional
Applicant
Sopro - Acteon Group
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/5/2014
Days to Decision
246 days
Submission Type
Statement