Medical Device Manufacturer · US , Mchenry , IL

Ausonics Pty , Ltd. - FDA 510(k) Cleared Devices

27 submissions · 26 cleared · Since 1979

Total

Cleared

Denied

Ausonics Pty , Ltd. has 26 FDA 510(k) cleared radiology devices. Based in Mchenry, US.

Historical record: 26 cleared submissions from 1979 to 1994.

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 - Ausonics Pty , Ltd.

27 devices

1-12 of 27

Cleared Oct 03, 1994

AUSONICS OPUS 2 REALTIME ULTRASOUND SCANNER

K933916 · IYN

Radiology · 418d

Cleared Jul 02, 1992

CINE RECALL FUNCTION/OPUS 1 REAL TIME SCANNER

K915715 · IYO

Radiology · 268d

Cleared May 19, 1992

AUSONICS OPUS 1 SYSTEM, ANNULAR ARRAY OPTION

K920307 · ITX

Radiology · 117d

Cleared Dec 18, 1991

DOPPLER UPGRADE FOR AUSONICS OPUS 1 REAL TIME SCAN

K905488 · LMB

Radiology · 376d

Cleared Feb 13, 1991

7.5 MHZ BI PLANE RECTAL PROBE (P/N: 041-815)

RESUBMITTAL OF MI 1000C MICROIMAGER

K881979 · JOP

Cardiovascular · 396d

Cleared Jan 10, 1989

APA-C CATALOG NUMBER A-8001-C

WWDS-005 HUMAN RECTAL PROBE

K883079 · IYO

Radiology · 146d

Cleared Nov 25, 1988

ALPHA MC-9S MOBIL C-ARM IMAGE INTENSIFIER UNIT

K883372 · JAA

Radiology · 107d

Cleared Jan 30, 1987

ALPHA II DIAGNOSTIC X-RAY

K864958 · IZH

Radiology · 43d

Ausonics Pty , Ltd. - FDA 510(k) Cleared Devices

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