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FDA 510(k) Applications Submitted by Jessie Duong
FDA 510(k) Number
Submission Date
Device Name
Applicant
K210088
01/13/2021
1688 4K Camera System, L11 LED Light Source with AIM, AIM SafeLight Cable, AIM Laparoscopes
Stryker
K150494
02/25/2015
Proteus Digital Health Feedback Device
PROTEUS DIGITAL HEALTH, INC.
K211202
04/22/2021
1688 4K Camera System, L11 LED Light Source with AIM, AIM SafeLight Cable, Precision S 4K Sinuscopes
Stryker
K191102
04/25/2019
Precision S 4K Sinuscope
Stryker
K183470
12/14/2018
Precision Ideal Eyes Arthroscopes
Stryker
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