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ACCUCORE SINGLE ACTION CORE BIOPSY DEVICE

Page Type
Cleared 510(K)
510(k) Number
K000612
510(k) Type
Traditional
Applicant
INRAD
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/24/2000
Days to Decision
61 days
Submission Type
Summary

ACCUCORE SINGLE ACTION CORE BIOPSY DEVICE

Page Type
Cleared 510(K)
510(k) Number
K000612
510(k) Type
Traditional
Applicant
INRAD
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/24/2000
Days to Decision
61 days
Submission Type
Summary