FDA 510(k) Substantially Equivalent 🇯🇵 Japan

MODEL SSD-710

K Number: K827285 · Decision Apr 21, 1982
Classifications
0
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
39
Review Days
22

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Basic Information

Device Name
MODEL SSD-710
K Number
K827285
Clearance Type
Traditional
Decision
Substantially Equivalent
Applicant
Aloka Co., Ltd.
Date Received
March 30, 1982
Decision Date
April 21, 1982
Advisory Committee
Unknown
Review Advisory Committee
RA
Third Party
N

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K081843 ULTRASOUND DATA ANALYSIS SYSTEM, MODEL DAS-RS1
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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
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