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Precision Point Biopsy Needle Guide

Page Type
Cleared 510(K)
510(k) Number
K160414
510(k) Type
Traditional
Applicant
Corbin Clinical Resources, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/1/2016
Days to Decision
167 days
Submission Type
Summary

Precision Point Biopsy Needle Guide

Page Type
Cleared 510(K)
510(k) Number
K160414
510(k) Type
Traditional
Applicant
Corbin Clinical Resources, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/1/2016
Days to Decision
167 days
Submission Type
Summary