FDA 510(k) FDA class 2 Substantially Equivalent 🇯🇵 Japan

Ultrasound System SONIMAGE HS1

K Number: K182153 · Decision Sep 6, 2018
Classifications
1
FEI Numbers
348
Registration Numbers
349
Same Product Code
892
Applicant Total
25
Review Days
29

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Basic Information

Device Name
Ultrasound System SONIMAGE HS1
K Number
K182153
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
892.1560
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Konica Minolta, Inc.
Date Received
August 8, 2018
Decision Date
September 6, 2018
Product Code
IYO
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
IYO System, Imaging, Pulsed Echo, Ultrasonic

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Other Clearances by Konica Minolta, Inc.

K Number Device Name
K250665 SKR 3000
K241319 SKR 3000
K240281 Bone Suppression Software
K230906 Konicaminolta DI-X1
K223267 SKR 3000
K220993 Ultrasound System SONIMAGE MX1
K213908 SKR 3000
K212685 KONICAMINOLTA DI-X1
K210619 SKR 3000
K210066 ImagePilot
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