Last synced on 14 November 2025 at 11:06 pm

CleverLock Guidewire Locking Device and Biopsy Cap

Page Type
Cleared 510(K)
510(k) Number
K190164
510(k) Type
Traditional
Applicant
Olympus Surgical Technologies America
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/4/2019
Days to Decision
63 days
Submission Type
Summary

CleverLock Guidewire Locking Device and Biopsy Cap

Page Type
Cleared 510(K)
510(k) Number
K190164
510(k) Type
Traditional
Applicant
Olympus Surgical Technologies America
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/4/2019
Days to Decision
63 days
Submission Type
Summary