Medison America, Inc.
Medison America, Inc. holds FDA 510(k) medical device clearances, first cleared 1993, most recent 2003.
Top product codes for Medison America, Inc.
Recent clearances by Medison America, Inc.
- K032329 — SA 9900 PLUS DIAGNOSTIC ULTRASOUND SYSTEM
- K031552 — MYCOLOR 202 DIAGNOSTIC ULTRASOUND SYSTEM AND TRANSDUCERS
- K013627 — SONOACE SA-8000 DIAGNOSTIC ULTRASOUND SYSTEM
- K012867 — SONOACE 9900 DIAGNOSTIC ULTRASOUND SYSTEM
- K012887 — SA6000II DIAGNOSTIC ULTRASOUND SYSTEM
- K003525 — VOLUSON 730 DIAGNOSTIC ULTRASOUND SYSTEM
- K003121 — MYSONO 201 DIAGNOSTIC ULTRASOUND AND TRANSDUCERS
- K002185 — SONOACE SA 9900 DIAGNOSTIC ULTRASOUND SYSTEM
- K000030 — SONOACE 600 DIAGNOSTIC ULTRASOUND SYSTEM
- K993517 — COMBISON 530D/VOLUSON 530D, TISSUE HARMONIC IMAGING (THI) OPTION
- K992761 — SONOACE 5500 DIAGNOSTIC ULTRASOUND SYSTEM
- K984639 — THE S-VNA 5-8(B) DIAGNOSTIC ULTRASOUND TRANSDUCER
- K992155 — VOLUSION SMALL PARTS TRANSDUCER, MODEL S-VNW 5-10, VOLUSION ABDOMINAL TRANSDUCER, MODEL S-VAW 4-7
- K990970 — SONOACE 6000C DIAGNOSTIC ULTRASOUND SYSTEM AND TRANSDUCERS, ALSO CALLED ULTRASOUND SYSTEM AND TRANSDUCERS
- K974813 — COMBISON 530D WITH POWER DOPPLER MODE
- K974269 — SA8800 DIAGNOSTIC ULTRASOUND SYSTEM AND TRANSDUCERS,
- K981510 — SONOACE 6000/ ULTRAMARK 400
- K940942 — COMBISON 530 DIAGNOSTIC ULTRASOUND SCANNER
- K953773 — 6.5 MHZ ENDORECTAL CONVEX ARRAY (10R) PROBE
- K925582 — MEDISON 4800
- K930579 — MEDISON 88P DIAGNOSTIC ULTRASOUND IMAGING SYTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.