Class Class II

SIRIUS Endoscope System (PR-SI-1230) (K250939)

K250939 2025-08-29 Traditional
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Description

SIRIUS Endoscope System (PR-SI-1230) by Precision Robotics (Hong Kong) Limited, an FDA 510(k) cleared obstetrics/gynecology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK250939
Clearance Date2025-08-29
Clearance TypeTraditional
Product CodeHET
Regulation Number884.1720

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