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

ALOKA PROSOUND ALPHA 6 DIAGNOSTIC ULTRASOUND SYSTEM

K Number: K093488 · Decision Nov 20, 2009
Classifications
1
FEI Numbers
348
Registration Numbers
349
Same Product Code
892
Applicant Total
39
Review Days
10

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Basic Information

Device Name
ALOKA PROSOUND ALPHA 6 DIAGNOSTIC ULTRASOUND SYSTEM
K Number
K093488
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1560
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Aloka Co., Ltd.
Date Received
November 10, 2009
Decision Date
November 20, 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 Aloka Co., Ltd.

K Number Device Name
K111227 ALOKA SSD-3500 DIAGNOSTIC ULTRASOUND SYSTEM
K110207 ALOKA PROUSOUND F75 DIAGNOSTIC ULTRASOUND SYSTEM
K083254 ALOKA PROUSOUND 2 DIAGNOSTIC ULTRASOUND SYSTEM
K081843 ULTRASOUND DATA ANALYSIS SYSTEM, MODEL DAS-RS1
K080176 ALOKA PROSOUND 6 DIAGNOSTIC ULTRASOUND SYSTEM
K072285 ALOKA SSD-ALPHA 7 ULTRASOUND SYSTEM
K060059 ALOKA SD-3500 ULTRASOUND SYSTEM
K043196 ALOKA SSD-ALPHA 10 ULTRASOUND SYSTEM
K040719 ALOKA MODEL SSD-4000 DIAGNOSTIC ULTRASOUND SYSTEM W/OPTIONAL SONOREAL 3D SYSTEM ACCESSORY
K033311 ALOKA SSD-5000 V5.0 ULTRASOUND SYSTEM
Search all 39 clearances from Aloka Co., Ltd. →