Class Class II

Sonosite LX and Sonosite PX Ultrasound Systems (K251106)

K251106 2025-08-29 Traditional
Home/ Devices/ Sonosite LX and Sonosite…

Description

Sonosite LX and Sonosite PX Ultrasound Systems by Fujifilm Sonosite, Inc., an FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK251106
Clearance Date2025-08-29
Clearance TypeTraditional
Product CodeIYN
Regulation Number892.1550

Categories

Need More Information?

Contact the manufacturer or request a quote for this device.

Request Quote
Scroll to Top