Last synced on 14 November 2025 at 11:06 pm

GenCut Core Biopsy System

Page Type
Cleared 510(K)
510(k) Number
K142839
510(k) Type
Traditional
Applicant
Covidien LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/29/2015
Days to Decision
211 days
Submission Type
Summary

GenCut Core Biopsy System

Page Type
Cleared 510(K)
510(k) Number
K142839
510(k) Type
Traditional
Applicant
Covidien LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/29/2015
Days to Decision
211 days
Submission Type
Summary