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IONOLUX PRO

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K102450
510(k) Type
Special
Applicant
Voco GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
10/8/2010
Days to Decision
42 days
Submission Type
Statement

IONOLUX PRO

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K102450
510(k) Type
Special
Applicant
Voco GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
10/8/2010
Days to Decision
42 days
Submission Type
Statement