Last synced on 14 November 2025 at 11:06 pm

AcuSee AS-P1000 System

Page Type
Cleared 510(K)
510(k) Number
K202119
510(k) Type
Traditional
Applicant
Weipeng (Suzhou) Medical Devices Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
10/7/2020
Days to Decision
69 days
Submission Type
Summary

AcuSee AS-P1000 System

Page Type
Cleared 510(K)
510(k) Number
K202119
510(k) Type
Traditional
Applicant
Weipeng (Suzhou) Medical Devices Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
10/7/2020
Days to Decision
69 days
Submission Type
Summary