Last synced on 10 January 2025 at 11:05 pm

LUDWIG Electrosurgical Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221574
510(k) Type
Traditional
Applicant
Aesthetics Biomedical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/16/2022
Days to Decision
137 days
Submission Type
Summary

LUDWIG Electrosurgical Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221574
510(k) Type
Traditional
Applicant
Aesthetics Biomedical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/16/2022
Days to Decision
137 days
Submission Type
Summary