Class Class II

ACUSON Sequoia Diagnostic Ultrasound System, ACUSON Sequoia Select Diagnostic Ultrasound System (K223735)

K223735 2023-02-06 Special
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Description

ACUSON Sequoia Diagnostic Ultrasound System, ACUSON Sequoia Select Diagnostic Ultrasound System by Siemens Medical Solutions USA, Inc. — FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK223735
Clearance Date2023-02-06
Clearance TypeSpecial
Product CodeIYN
Regulation Number892.1550

Categories

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