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

RADIATION TREATMENT FOR CANCER PATIENTS

K Number: K930182 · Decision Jan 5, 1994
Classifications
1
FEI Numbers
114
Registration Numbers
114
Same Product Code
733
Applicant Total
6
Review Days
356

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Basic Information

Device Name
RADIATION TREATMENT FOR CANCER PATIENTS
K Number
K930182
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.5050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Northwest Medical Physics Center
Date Received
January 14, 1993
Decision Date
January 5, 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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Other Clearances by Northwest Medical Physics Center

K Number Device Name
K953227 CASPER
K941118 HEAD IMMOBILIZATION APPARATUS
K933117 IORT SYSTEM
K944613 SHOULDER RETRACTOR
K904908 STEREOTACTIC IRRADIATION SYSTEM