Ausonics Pty , Ltd.
Ausonics Pty , Ltd. holds FDA 510(k) medical device clearances, first cleared 1979, most recent 1994.
Top product codes for Ausonics Pty , Ltd.
Recent clearances by Ausonics Pty , Ltd.
- K933916 — AUSONICS OPUS 2 REALTIME ULTRASOUND SCANNER
- K915715 — CINE RECALL FUNCTION/OPUS 1 REAL TIME SCANNER
- K920307 — AUSONICS OPUS 1 SYSTEM, ANNULAR ARRAY OPTION
- K905488 — DOPPLER UPGRADE FOR AUSONICS OPUS 1 REAL TIME SCAN
- K902728 — 7.5 MHZ BI PLANE RECTAL PROBE (P/N: 041-815)
- K896714 — AUSONICS 5000
- K881979 — RESUBMITTAL OF MI 1000C MICROIMAGER
- K884299 — APA-C CATALOG NUMBER A-8001-C
- K883925 — UROIMAGER
- K883079 — WWDS-005 HUMAN RECTAL PROBE
- K883372 — ALPHA MC-9S MOBIL C-ARM IMAGE INTENSIFIER UNIT
- K864958 — ALPHA II DIAGNOSTIC X-RAY
- K863710 — ALPHA S/D DIAGNOSTIC X-RAY MAMMOGRAPHY UNIT
- K862166 — SONORANGER
- K862627 — SONORANGER TRANSVAGINAL PROBE
- K860494 — 7.5 MHZ SHORT FOCUS FLUID OFFSET PROBE #041-726T
- K852549 — SONORANGER
- K851616 — 3.5. MHZ PROBE FOR AUSONICS 150 & 357 REAL TIME CA
- K851696 — AUSONICS 150
- K843971 — AUSONICS 150
- K843994 — AUSONICS 357
- K850173 — AUSONICS-ALPHA I DIAGNOSTIC X-RAY MAMMOGRAPHY UNIT
- K837171 — ULTRASONIC ECHOSCOPE
- K811633 — CIRAS ULTRASONIC SCANNING SYSTEM
- K801675 — U.I. OCTOSON
- K802030 — U.I. OCTOSON
- K792388 — OCTOSON
Data sourced from openFDA. This site is unofficial and independent of the FDA.