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SURECORE BIOPSY DEVICE

Page Type
Cleared 510(K)
510(k) Number
K102756
510(k) Type
Traditional
Applicant
CHEST INNOVATIONS INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/29/2011
Days to Decision
432 days
Submission Type
Summary

SURECORE BIOPSY DEVICE

Page Type
Cleared 510(K)
510(k) Number
K102756
510(k) Type
Traditional
Applicant
CHEST INNOVATIONS INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/29/2011
Days to Decision
432 days
Submission Type
Summary