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

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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