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

SHIMADZU X-RAY HIGH-VOLTAGE GENERATOR XUD150K

K Number: K911339 · Decision Apr 16, 1991
Classifications
1
FEI Numbers
42
Registration Numbers
42
Same Product Code
162
Applicant Total
90
Review Days
21

Basic Information

Device Name
SHIMADZU X-RAY HIGH-VOLTAGE GENERATOR XUD150K
K Number
K911339
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
892.1700
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Shimadzu Medical Systems
Date Received
March 26, 1991
Decision Date
April 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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K082224 DIAGNOSTIC ULTRASOUND SYSTEM SARANO, ECHO VIEW, SHIMASONIC
K071287 ECHOVIEW / SHIMASONIC DIAGNOSTIC ULTRASOUND DEVICE, MODEL SDU-2200PRO
K071289 ECHOVIEW / SHIMASONIC DIAGNOSTIC ULTRASOUND SYSTEM, MODEL SDU-1200PRO
K071291 ECHOVIEW / SHIMASONIC DIAGNOSTIC ULTRASOUND SYSTEM, MODEL SDU-1100
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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