FDA 510(k) Substantially Equivalent 🇺🇸 United States

ARS-1000 RADIATION THERAPY TREATMENT PLANNING SYSTEM

K Number: K827175 · Decision Mar 31, 1982
Classifications
0
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
2
Review Days
41

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Basic Information

Device Name
ARS-1000 RADIATION THERAPY TREATMENT PLANNING SYSTEM
K Number
K827175
Clearance Type
Traditional
Decision
Substantially Equivalent
Applicant
Applied Radiation
Date Received
February 18, 1982
Decision Date
March 31, 1982
Advisory Committee
Unknown
Review Advisory Committee
RA
Third Party
N

Other Clearances by Applied Radiation

K Number Device Name
K820448 ARS-1000