Class Class II

EdgeLife Handheld Wireless Ultrasound System (E8200); EdgeLife Handheld Wireless Ultrasound System (E8220) (K234153)

K234153 2024-09-18 Traditional
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Description

EdgeLife Handheld Wireless Ultrasound System (E8200); EdgeLife Handheld Wireless Ultrasound System (E8220) by Edgelife Technologies, LLC — FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK234153
Clearance Date2024-09-18
Clearance TypeTraditional
Product CodeIYN
Regulation Number892.1550

Categories

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