Class Class II

TE Air Diagnostic Ultrasound System (K240906)

K240906 2024-07-23 Traditional
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Description

TE Air Diagnostic Ultrasound System by Shenzhen Mindray Bio-Medical Electronics Co., Ltd. — FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK240906
Clearance Date2024-07-23
Clearance TypeTraditional
Product CodeIYN
Regulation Number892.1550

Categories

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