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MyoSure XL Tissue Removal Device for Fluent

Page Type
Cleared 510(K)
510(k) Number
K181974
510(k) Type
Special
Applicant
Hologic, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/23/2018
Days to Decision
30 days
Submission Type
Summary

MyoSure XL Tissue Removal Device for Fluent

Page Type
Cleared 510(K)
510(k) Number
K181974
510(k) Type
Special
Applicant
Hologic, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/23/2018
Days to Decision
30 days
Submission Type
Summary