FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

AUSONICS 5000

K Number: K896714 · Decision Jun 11, 1990
Classifications
1
FEI Numbers
345
Registration Numbers
346
Same Product Code
883
Applicant Total
27
Review Days
194

Basic Information

Device Name
AUSONICS 5000
K Number
K896714
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1560
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
AUSONICS PTY LTD.
Date Received
November 29, 1989
Decision Date
June 11, 1990
Product Code
IYO
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
IYO System, Imaging, Pulsed Echo, Ultrasonic

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (IYO), ordered by most recent decision date.

View all

Other Clearances by AUSONICS PTY LTD.

K Number Device Name
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)
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
Search all 27 clearances from AUSONICS PTY LTD. →