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SANARUS INCORE ROTATIONAL CORE BIOPSY DEVICE, MODELS CB3010, CB3012

Page Type
Cleared 510(K)
510(k) Number
K080171
510(k) Type
Traditional
Applicant
SANARUS MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/6/2008
Days to Decision
42 days
Submission Type
Summary

SANARUS INCORE ROTATIONAL CORE BIOPSY DEVICE, MODELS CB3010, CB3012

Page Type
Cleared 510(K)
510(k) Number
K080171
510(k) Type
Traditional
Applicant
SANARUS MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/6/2008
Days to Decision
42 days
Submission Type
Summary