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

LINEAR ACCELERATOR COLLIMATOR

K Number: K911973 · Decision Oct 15, 1992
Classifications
1
FEI Numbers
114
Registration Numbers
114
Same Product Code
733
Applicant Total
7
Review Days
531

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Basic Information

Device Name
LINEAR ACCELERATOR COLLIMATOR
K Number
K911973
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.5050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Medical Equipment Development Co., Inc.
Date Received
May 3, 1991
Decision Date
October 15, 1992
Product Code
IYE
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
IYE Accelerator, Linear, Medical

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