FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇳 China

GE LOGIQ I/E & VIVID E COMPACT ULTRASOUND

K Number: K091374 · Decision May 26, 2009
Classifications
1
FEI Numbers
348
Registration Numbers
349
Same Product Code
892
Applicant Total
12
Review Days
15

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Basic Information

Device Name
GE LOGIQ I/E & VIVID E COMPACT ULTRASOUND
K Number
K091374
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1560
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ge Medical Systems China Co., Ltd.
Date Received
May 11, 2009
Decision Date
May 26, 2009
Product Code
IYO
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
Y

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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Other Clearances by Ge Medical Systems China Co., Ltd.

K Number Device Name
K151063 Monitor B40
K142288 MAC 800 Resting ECG Analysis System
K133576 MONITOR B40
K130584 MONITOR B40
K122253 PROCARE MONITOR B20
K123238 ACHILLES
K120598 PROCARE MONITOR B40
K103633 ACHILLES
K102256 GE LOGIQ I/E & VIVID E COMPACT DIAGNOSTIC ULTRASOUND
K102113 GE VENUE 40 COMPACT DIAGNOSTIC ULTRASOUND
Search all 12 clearances from Ge Medical Systems China Co., Ltd. →