Last synced on 14 November 2025 at 11:06 pm

EndoScreener

Page Type
Cleared 510(K)
510(k) Number
K211326
510(k) Type
Traditional
Applicant
Chengdu Wision Medical Device Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
11/19/2021
Days to Decision
203 days
Submission Type
Summary

EndoScreener

Page Type
Cleared 510(K)
510(k) Number
K211326
510(k) Type
Traditional
Applicant
Chengdu Wision Medical Device Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
11/19/2021
Days to Decision
203 days
Submission Type
Summary