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

AU5, AU6

K Number: K000681 · Decision May 3, 2000
Classifications
1
FEI Numbers
345
Registration Numbers
346
Same Product Code
883
Applicant Total
20
Review Days
65

Basic Information

Device Name
AU5, AU6
K Number
K000681
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1560
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
BIOSOUND ESAOTE, INC.
Date Received
February 28, 2000
Decision Date
May 3, 2000
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

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K020164 E-SCAN XQ
K012728 E-SCAN MRI SYSTEM
K010405 7230 ULTRASOUND IMAGING SYSTEM WITH TEI
K010057 MODIFICATION TO ARTOSCAN M
K001894 MODIFICATION TO E-SCAN
K000931 AU5 ULTRASOUND IMAGING SYSTEM
K994369 7250 (MEGAS)
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