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

SONOVIEW PRO BY MEDISON CO., LTD.

K Number: K031886 · Decision Jun 30, 2003
Classifications
1
FEI Numbers
609
Registration Numbers
609
Same Product Code
2221
Applicant Total
24
Review Days
12

Basic Information

Device Name
SONOVIEW PRO BY MEDISON CO., LTD.
K Number
K031886
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
MEDISON CO., LTD.
Date Received
June 18, 2003
Decision Date
June 30, 2003
Product Code
LLZ
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
LLZ System, Image Processing, Radiological

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LLZ), ordered by most recent decision date.

View all

Other Clearances by MEDISON CO., LTD.

K Number Device Name
K103397 ACCUVIX XG DIAGNOSTIC ULTRASOUND SYSTEM
K103722 THE SONOACE R5 DIAGNOSTIC ULTRASOUND SYSTEM
K102065 SONOACE R7 DIAGNOSTIC ULTRASOUND SYSTEM
K101455 EKO 7 DIAGNOSTIC ULTRASOUND SYSTEM
K101829 THE SONOACE R3 DIAGNOSTIC ULTRASOUND SYSTEM
K100186 MYSONO U5 DIAGNOSTIC ULTRASOUND SYSTEM
K093849 ACCUVIX V10 DIAGNOSTIC ULTRASOUND SYSTEM
K093714 SONOACE X8 DIAGNOSTIC ULTRASOUND SYSTEM
K092159 ACCUVIX V20 DIAGNOSTIC ULTRASOUND SYSTEM
K081676 SONOACE X6 DIAGNOSTIC ULTRASOUND SYSTEM
Search all 24 clearances from MEDISON CO., LTD. →