Last synced on 14 November 2025 at 11:06 pm

V12 PRO

Page Type
Cleared 510(K)
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)
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