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

3.5. MHZ PROBE FOR AUSONICS 150 & 357 REAL TIME CA

K Number: K851616 · Decision Jul 29, 1985
Classifications
1
FEI Numbers
16
Registration Numbers
16
Same Product Code
71
Applicant Total
27
Review Days
102

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Basic Information

Device Name
3.5. MHZ PROBE FOR AUSONICS 150 & 357 REAL TIME CA
K Number
K851616
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2880
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Ausonics Pty , Ltd.
Date Received
April 18, 1985
Decision Date
July 29, 1985
Product Code
JOP
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

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

Product Code Device Name
JOP Transducer, Ultrasonic

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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. →