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

ALPHA II DIAGNOSTIC X-RAY

K Number: K864958 · Decision Jan 30, 1987
Classifications
1
FEI Numbers
26
Registration Numbers
26
Same Product Code
175
Applicant Total
27
Review Days
43

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
ALPHA II DIAGNOSTIC X-RAY
K Number
K864958
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1710
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Ausonics Pty , Ltd.
Date Received
December 18, 1986
Decision Date
January 30, 1987
Product Code
IZH
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
IZH System, X-Ray, Mammographic

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (IZH), 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)
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
Search all 27 clearances from Ausonics Pty , Ltd. →