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510(k) K251830

Sonosite LX Ultrasound System by FUJIFILM Sonosite, Inc. — Product Code IYN

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 10, 2025
Date Received
June 13, 2025
Clearance Type
Traditional
Expedited Review
No
Third Party Review
Yes

Device Classification

Device Name
System, Imaging, Pulsed Doppler, Ultrasonic
Device Class
Class II
Regulation Number
892.1550
Review Panel
RA
Submission Type

Other clearances by FUJIFILM Sonosite, Inc.

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  • K251106 — Sonosite LX and Sonosite PX Ultrasound Systems (August 29, 2025)
  • K233597 — Sonosite LX Ultrasound System (December 6, 2023)
  • K213763 — Sonosite PX Ultrasound System (December 27, 2021)
  • K202160 — Sonosite PX Ultrasound System, Sonosite SII Ultrasound System, Sonosite iViz Ult (September 1, 2020)
  • K200964 — Sonosite PX Ultrasound System (May 8, 2020)
  • K190476 — FUJIFILM Sonosite Vevo MD Imaging System (March 15, 2019)
  • K183235 — SonoSite SII Ultrasound System (February 7, 2019)
  • K180704 — SonoSite iViz Ultrasound System (April 13, 2018)

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