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

IVR MASTER

K Number: K945389 · Decision Feb 7, 1995
Classifications
1
FEI Numbers
609
Registration Numbers
609
Same Product Code
2221
Applicant Total
49
Review Days
96

Basic Information

Device Name
IVR MASTER
K Number
K945389
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
SHIMADZU CORP.
Date Received
November 3, 1994
Decision Date
February 7, 1995
Product Code
LLZ
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
LLZ System, Image Processing, Radiological

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