Medical Device Manufacturer · US , Fremont , CA

Medison America, Inc. - FDA 510(k) Cleared Devices

21 submissions · 21 cleared · Since 1993
21
Total
21
Cleared
0
Denied

Medison America, Inc. has 21 FDA 510(k) cleared radiology devices. Based in Fremont, US.

Historical record: 21 cleared submissions from 1993 to 2003.

Browse the complete list of FDA 510(k) cleared radiology devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Medison America, Inc.
21 devices
1-12 of 21
Cleared Aug 06, 2003
SA 9900 PLUS DIAGNOSTIC ULTRASOUND SYSTEM
K032329 · IYN
Radiology · 8d
Cleared May 30, 2003
MYCOLOR 202 DIAGNOSTIC ULTRASOUND SYSTEM AND TRANSDUCERS
K031552 · IYN
Radiology · 11d
Cleared Nov 16, 2001
SONOACE SA-8000 DIAGNOSTIC ULTRASOUND SYSTEM
K013627 · IYN
Radiology · 11d
Cleared Sep 12, 2001
SONOACE 9900 DIAGNOSTIC ULTRASOUND SYSTEM
K012867 · IYN
Radiology · 16d
Cleared Sep 12, 2001
SA6000II DIAGNOSTIC ULTRASOUND SYSTEM
K012887 · IYO
Radiology · 15d
Cleared Nov 22, 2000
VOLUSON 730 DIAGNOSTIC ULTRASOUND SYSTEM
K003525 · IYN
Radiology · 7d
Cleared Oct 20, 2000
MYSONO 201 DIAGNOSTIC ULTRASOUND AND TRANSDUCERS
K003121 · IYO
Radiology · 15d
Cleared Aug 01, 2000
SONOACE SA 9900 DIAGNOSTIC ULTRASOUND SYSTEM
K002185 · IYN
Radiology · 13d
Cleared Jan 19, 2000
SONOACE 600 DIAGNOSTIC ULTRASOUND SYSTEM
K000030 · IYO
Radiology · 14d
Cleared Nov 02, 1999
COMBISON 530D/VOLUSON 530D, TISSUE HARMONIC IMAGING (THI) OPTION
K993517 · IYO
Radiology · 15d
Cleared Sep 01, 1999
SONOACE 5500 DIAGNOSTIC ULTRASOUND SYSTEM
K992761 · IYO
Radiology · 15d
Cleared Jul 12, 1999
THE S-VNA 5-8(B) DIAGNOSTIC ULTRASOUND TRANSDUCER
K984639 · ITX
Radiology · 193d
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