FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

SHIMADZU X-RAY HIGH VOLTAGE GENERATOR UD150L

K Number: K913065 · Decision Sep 16, 1991
Classifications
1
FEI Numbers
45
Registration Numbers
45
Same Product Code
162
Applicant Total
90
Review Days
68

Basic Information

Device Name
SHIMADZU X-RAY HIGH VOLTAGE GENERATOR UD150L
K Number
K913065
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
892.1700
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
SHIMADZU MEDICAL SYSTEMS
Date Received
July 10, 1991
Decision Date
September 16, 1991
Product Code
IZO
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
IZO Generator, High-Voltage, X-Ray, Diagnostic

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K071291 ECHOVIEW / SHIMASONIC DIAGNOSTIC ULTRASOUND SYSTEM, MODEL SDU-1100
K071289 ECHOVIEW / SHIMASONIC DIAGNOSTIC ULTRASOUND SYSTEM, MODEL SDU-1200PRO
K061643 ECHO VIEW/SHIMASONIC DIAGNOSTIC ULTRASOUND SYSTEM, MODEL SDU-1200PRO
K061637 ECHOVIEW/ SHIMASONIC DIAGNOSTIC ULTRASOUND SYSTEM, MODEL SDU-2200PRO
K061641 ECHO VIEW/SHIMASONIC DIAGNOSTIC ULTRASOUND SYSTEM, MODEL SARANO
K052500 DAR-8000F
K052076 DAR-8000I
K050510 ECHOVIEW/SHIMASONIC DIAGNOSTIC ULTRASOUND SYSTEM, MODEL SDU-1100
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