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Mammotome Revolve Dual Vacuum Assisted Biopsy (VAB) System

Page Type
Cleared 510(K)
510(k) Number
K202012
510(k) Type
Traditional
Applicant
Devicor Medical Products, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/18/2020
Days to Decision
28 days
Submission Type
Summary

Mammotome Revolve Dual Vacuum Assisted Biopsy (VAB) System

Page Type
Cleared 510(K)
510(k) Number
K202012
510(k) Type
Traditional
Applicant
Devicor Medical Products, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/18/2020
Days to Decision
28 days
Submission Type
Summary