Last synced on 16 May 2025 at 11:05 pm

V12 PRO

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K210913
510(k) Type
Traditional
Applicant
SLK Medical GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
8/4/2021
Days to Decision
128 days
Submission Type
Summary

V12 PRO

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K210913
510(k) Type
Traditional
Applicant
SLK Medical GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
8/4/2021
Days to Decision
128 days
Submission Type
Summary