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Mammotome revolve Dual Vacuum Assist Biopsy System

Page Type
Cleared 510(K)
510(k) Number
K152989
510(k) Type
Traditional
Applicant
DEVICOR MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/25/2016
Days to Decision
135 days
Submission Type
Summary

Mammotome revolve Dual Vacuum Assist Biopsy System

Page Type
Cleared 510(K)
510(k) Number
K152989
510(k) Type
Traditional
Applicant
DEVICOR MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/25/2016
Days to Decision
135 days
Submission Type
Summary