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MCL 31 Dermablate System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K210634
510(k) Type
Traditional
Applicant
Asclepion Laser Technologies GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
4/13/2022
Days to Decision
406 days
Submission Type
Summary

MCL 31 Dermablate System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K210634
510(k) Type
Traditional
Applicant
Asclepion Laser Technologies GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
4/13/2022
Days to Decision
406 days
Submission Type
Summary