Last synced on 22 September 2023 at 11:04 pm

MultiCut Solo

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213597
510(k) Type
Traditional
Applicant
Asclepion Laser Technologies GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
1/18/2023
Days to Decision
432 days
Submission Type
Summary