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

LOGIQ P9; LOGIQ P7

K Number: K181783 · Decision Sep 20, 2018
Classifications
1
FEI Numbers
211
Registration Numbers
211
Same Product Code
1117
Applicant Total
47
Review Days
79

Basic Information

Device Name
LOGIQ P9; LOGIQ P7
K Number
K181783
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1550
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
GE Healthcare
Date Received
July 3, 2018
Decision Date
September 20, 2018
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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