FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇦 Canada

THERAPLAN PLUS VERSION 1.2

K Number: K970236 · Decision Jul 9, 1997
Classifications
1
FEI Numbers
114
Registration Numbers
114
Same Product Code
733
Applicant Total
9
Review Days
169

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Basic Information

Device Name
THERAPLAN PLUS VERSION 1.2
K Number
K970236
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.5050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Theratronics, Inc.
Date Received
January 21, 1997
Decision Date
July 9, 1997
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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Other Clearances by Theratronics, Inc.

K Number Device Name
K983917 THERATRON ELITE
K964606 THERATRON 780E
K964607 THERATON 1000E
K954679 THERAPLAN PLUS
K940237 THERAPLAN V05B/ TP-11 V09B
K922276 THERAC 25
K894165 THERATRON 1000
K820782 THERATRONIC STIMULATOR