Class Class II

ULTRASONIC PROBE UM-3R (UM-3R); ULTRASONIC PROBE UM-G20-29R (UM-G20-29R) (K250883)

K250883 2025-09-18 Traditional
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Description

ULTRASONIC PROBE UM-3R (UM-3R); ULTRASONIC PROBE UM-G20-29R (UM-G20-29R) by Olympus Medical Systems Corporation, an FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK250883
Clearance Date2025-09-18
Clearance TypeTraditional
Product CodeITX
Regulation Number892.1570

Categories

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