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

THERAC 25

K Number: K922276 · Decision May 25, 1994
Classifications
1
FEI Numbers
123
Registration Numbers
124
Same Product Code
717
Applicant Total
9
Review Days
740

Basic Information

Device Name
THERAC 25
K Number
K922276
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.5050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
THERATRONICS, INC.
Date Received
May 15, 1992
Decision Date
May 25, 1994
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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