Class Class II

Arthrex SynergyID Endoscopic Imaging System (K223759)

K223759 2023-02-24 Traditional
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Description

Arthrex SynergyID Endoscopic Imaging System by Arthex, Inc. — FDA 510(k) cleared gastroenterology, urology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK223759
Clearance Date2023-02-24
Clearance TypeTraditional
Product CodeGCJ
Regulation Number876.1500

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