Sonosite,Inc.
FDA 510(k) medical device clearances.
Top product codes for Sonosite,Inc.
Recent clearances by Sonosite,Inc.
- K113156 — SONOSITE EDGE ULTRASOUND SYSTEM
- K110645 — BIO Z CARDIO PROFILE HEMODYNAMIC MONITOR
- K102390 — SONOSITE NANOMAXX SERIES ULTRASOUND SYSTEM
- K093510 — LUMENVU CATHETER GUIDANCE SYSTEM
- K101757 — SONOSITE NANOMAXX SERIES ULTRASOUND SYSTEM, SONOSITE MAXX SERIES ULTRASOUND SYSTEM
- K092058 — SONOSITE NANOMAXX SERIES ULTRASOUND SYSTEM
- K082098 — SONOSITE MAXX SERIES ULTRASOUND SYSTEM
- K071134 — SONOSITE MAXX SERIES DIAGNOSTIC ULTRASOUND SYSTEM
- K053069 — SONOSITE MICROMAXX DIAGNOSTIC ULTRASOUND SYSTEM (C3 SERIES)
- K052109 — SONOSITE HAND-CARRIED ULTRASOUND SYSTEM (C1 SERIES)
- K043559 — SONOSITE HIGH-RESOLUTION DIAGNOSTIC ULTRASOUND SYSTEM (C3 SERIES)
- K043452 — TITAN HIGH RESOLUTION ULTRASOUND SYSTEM AND SONOSITE ULTRASOUND SYSTEM
- K033367 — TITAN ULTRASOUND SYSTEM, SONOSITE ILOOK 25 ULTRASOUND SYSTEM, 180PLUS ULTRASOUND SYSTEM, MODEL L03073, L02245, L02464
- K030949 — TITAN HIGH RESOLUTION ULTRASOUND SYSTEM
- K030064 — ILOOK 25 NEEDLE GUIDE ATTACHMENT AND BRACKET ASSEMBLY
- K023957 — SONOSITE HAND-CARRIED ULTRASOUND SYSTEM (C2 SERIES)
- K021628 — SONOSITE HAND-CARIED UNTRASOUND SYSTEM (POWERSERIES)
- K014116 — HAND-CARRIED ULTRASOUND SYSTEM
- K010374 — SONOSITE HAND-CARRIED ULTRASOUND SYSTEM
- K003399 — SONOSITE HAND-CARRIED ULTRASOUND SYSTEM
- K994096 — SONOHEART HAND-CARRIED ECHOCARDIOGRAPHY SYSTEM
- K990806 — C1 ULTRASOUND SYSTEM
- K981505 — COZUMEL DIAGNOSTIC ULTRASOUND SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.