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LUDWIG Electrosurgical Device

Page Type
Cleared 510(K)
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)
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