FUJIFILM Sonosite, Inc.
FUJIFILM Sonosite, Inc. holds FDA 510(k) medical device clearances, first cleared 2013, most recent 2026.
Top product codes for FUJIFILM Sonosite, Inc.
Recent clearances by FUJIFILM Sonosite, Inc.
- K260595 — Sonosite iLOOK Ultrasound System
- K253448 — Sonosite MT Ultrasound System
- K251106 — Sonosite LX and Sonosite PX Ultrasound Systems
- K251830 — Sonosite LX Ultrasound System
- K233597 — Sonosite LX Ultrasound System
- K213763 — Sonosite PX Ultrasound System
- K202160 — Sonosite PX Ultrasound System, Sonosite SII Ultrasound System, Sonosite iViz Ultrasound System, Sonosite X-Porte Ultrasound System, Sonosite Edge II Ultrasound System, Sonosite Maxx Ultrasound System
- K200964 — Sonosite PX Ultrasound System
- K190476 — FUJIFILM Sonosite Vevo MD Imaging System
- K183235 — SonoSite SII Ultrasound System
- K180704 — SonoSite iViz Ultrasound System
- K171437 — SonoSite X-Porte Ultrasound System
- K162288 — SonoSite iViz Ultrasound System
- K162045 — SonoSite SII Ultrasound System, SonoSite Edge II Ultrasound System
- K161119 — SonoSite iViz Ultrasound System
- K160674 — Fujifilm Sonosite Vevo MD Imaging System
- K160734 — SonoSite SII Ultrasound System
- K160406 — FUJIFILM FC1 Ultrasound System
- K153626 — SonoSite Edge II Ultrasound System
- K152983 — FUJIFILM SonoSite iViz Ultrasound System
- K152209 — FUJIFILM SonoSite X-Porte Ultrasound System
- K142017 — X-PORTE ULTRASOUND SYSTEM
- K133454 — SONOSITE EDGE ULTRASOUND SYSTEM
- K133134 — X-PORTE ULTRASOUND SYSTEM
- K130173 — SONOSITE MAXX SERIES ULTRASOUND SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.