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CASSI II Rotational Core Biopsy System

Page Type
Cleared 510(K)
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)
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