FUJIFILM Sonosite, Inc.
FDA 510(k) medical device clearances.
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.