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

GE VIVID 7, MODEL FC0003XX

K Number: K031663 · Decision Jun 9, 2003
Classifications
1
FEI Numbers
211
Registration Numbers
211
Same Product Code
1117
Applicant Total
254
Review Days
11

Basic Information

Device Name
GE VIVID 7, MODEL FC0003XX
K Number
K031663
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
892.1550
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
GENERAL ELECTRIC CO.
Date Received
May 29, 2003
Decision Date
June 9, 2003
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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