Last synced on 14 November 2025 at 11:06 pm

PowerCube+ Series (PowerCube Body+); PowerCube+ Series (PowerCube Diffusion+); PowerCube+ Series (PowerCube Body+ / Diffusion+)

Page Type
Cleared 510(K)
510(k) Number
K240706
510(k) Type
Traditional
Applicant
Ganshorn Medizin Electronic GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
12/9/2024
Days to Decision
270 days
Submission Type
Summary

PowerCube+ Series (PowerCube Body+); PowerCube+ Series (PowerCube Diffusion+); PowerCube+ Series (PowerCube Body+ / Diffusion+)

Page Type
Cleared 510(K)
510(k) Number
K240706
510(k) Type
Traditional
Applicant
Ganshorn Medizin Electronic GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
12/9/2024
Days to Decision
270 days
Submission Type
Summary