Class Class II

X9 Ultrasound System (K251673)

K251673 2025-10-17 Traditional
Home/ Devices/ X9 Ultrasound System (K251673)

Description

X9 Ultrasound System by X9, Inc., an FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK251673
Clearance Date2025-10-17
Clearance TypeTraditional
Product CodeSGH
Regulation Number892.1560

Categories

Need More Information?

Contact the manufacturer or request a quote for this device.

Request Quote
Scroll to Top