Last synced on 14 November 2025 at 11:06 pm

PeriView FLEX

Page Type
Cleared 510(K)
510(k) Number
K171232
510(k) Type
Traditional
Applicant
Olympus Surgical Technologies America
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/21/2017
Days to Decision
147 days
Submission Type
Summary

PeriView FLEX

Page Type
Cleared 510(K)
510(k) Number
K171232
510(k) Type
Traditional
Applicant
Olympus Surgical Technologies America
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/21/2017
Days to Decision
147 days
Submission Type
Summary