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Electrosurgical accessory

Page Type
Cleared 510(K)
510(k) Number
K210394
510(k) Type
Traditional
Applicant
Dornier MedTech America Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/19/2021
Days to Decision
98 days
Submission Type
Summary

Electrosurgical accessory

Page Type
Cleared 510(K)
510(k) Number
K210394
510(k) Type
Traditional
Applicant
Dornier MedTech America Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/19/2021
Days to Decision
98 days
Submission Type
Summary