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

7230 ULTRASOUND IMAGING SYSTEM WITH TEI

K Number: K010405 · Decision Mar 13, 2001
Classifications
1
FEI Numbers
211
Registration Numbers
211
Same Product Code
1117
Applicant Total
20
Review Days
29

Basic Information

Device Name
7230 ULTRASOUND IMAGING SYSTEM WITH TEI
K Number
K010405
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1550
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
BIOSOUND ESAOTE, INC.
Date Received
February 12, 2001
Decision Date
March 13, 2001
Product Code
IYN
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
IYN System, Imaging, Pulsed Doppler, Ultrasonic

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