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

MEVATRON 74

K Number: K790747 · Decision May 4, 1979
Classifications
1
FEI Numbers
114
Registration Numbers
114
Same Product Code
733
Applicant Total
13
Review Days
18

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Basic Information

Device Name
MEVATRON 74
K Number
K790747
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.5050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Siemens Medical Laboratories, Inc.
Date Received
April 16, 1979
Decision Date
May 4, 1979
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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K882729 MEVATRON, M 2 CLASS
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K862339 MEVATRON KD-2
K854609 MEVAMATIC 3
K852907 SIEMENS MEVATRON ME
K812032 MEVATRON 67E
K791967 MEVATRON 74X MEDICAL LINEAR ACCELERATOR
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