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SANARUS INCORE ROTATIONAL CORE BIOPSY DEVICE, MODELS CB3010, CB3012

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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