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

RAPTOR TREATMENT PLANNING SYSTEM

K Number: K993359 · Decision Dec 21, 1999
Classifications
1
FEI Numbers
114
Registration Numbers
114
Same Product Code
733
Applicant Total
21
Review Days
76

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Basic Information

Device Name
RAPTOR TREATMENT PLANNING SYSTEM
K Number
K993359
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.5050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Nomos Corp.
Date Received
October 6, 1999
Decision Date
December 21, 1999
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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