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CASSI II Rotational Core Biopsy System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K161234
510(k) Type
Special
Applicant
Scion Medical Technologies, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/3/2016
Days to Decision
93 days
Submission Type
Summary

CASSI II Rotational Core Biopsy System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K161234
510(k) Type
Special
Applicant
Scion Medical Technologies, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/3/2016
Days to Decision
93 days
Submission Type
Summary