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OR340 INTRAOPERATIVE ULTRASOUND BIOPSY NEEDLE GUID

Page Type
Cleared 510(K)
510(k) Number
K913987
510(k) Type
Traditional
Applicant
Codman & Shurtleff, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/13/1992
Days to Decision
221 days
Submission Type
Summary

OR340 INTRAOPERATIVE ULTRASOUND BIOPSY NEEDLE GUID

Page Type
Cleared 510(K)
510(k) Number
K913987
510(k) Type
Traditional
Applicant
Codman & Shurtleff, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/13/1992
Days to Decision
221 days
Submission Type
Summary