Medical Device Manufacturer · US , Mchenry , IL

Diasonics, Inc. - FDA 510(k) Cleared Devices

42 submissions · 41 cleared · Since 1978

Total

Cleared

Denied

Diasonics, Inc. has 41 FDA 510(k) cleared radiology devices. Based in Mchenry, US.

Historical record: 41 cleared submissions from 1978 to 1997.

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 - Diasonics, Inc.

42 devices

1-12 of 42

Cleared Jan 02, 1997

VINGMED SOUND COLOR FLOW MAPPING SYSTEM

K962662 · IYO

Radiology · 178d

Cleared Sep 28, 1993

CFM-800 COLOR FLOW MAPPING SYSTEM

CW DOPPLER 2.25 MHZ PROBE

ACCESS(TM), SOFTWARE RELEASE 4.11P

K896637 · LPH

Radiology · 59d

Cleared Oct 27, 1989

MT/S SOFTWARE RELEASE 5.0.

SPECTRA ULTRASOUND SYSTEM W/COLOR FLOW MODULE

K891452 · IYO

Radiology · 84d

Cleared May 11, 1989

MAGNETIC RESONANCE DEVICE ACCESSORY SOFTWARE 4.0.

K891541 · LNH

Radiology · 55d

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Diasonics, Inc. - FDA 510(k) Cleared Devices

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