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

C-ARM TABLE IVS-100

K Number: K963888 · Decision Dec 18, 1996
Classifications
1
FEI Numbers
139
Registration Numbers
139
Same Product Code
297
Applicant Total
90
Review Days
83

Basic Information

Device Name
C-ARM TABLE IVS-100
K Number
K963888
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1650
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
SHIMADZU MEDICAL SYSTEMS
Date Received
September 26, 1996
Decision Date
December 18, 1996
Product Code
JAA
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
JAA System, X-Ray, Fluoroscopic, Image-Intensified

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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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