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

NUCLETRON PLANNING SYSTEM

K Number: K911612 · Decision Jun 13, 1991
Classifications
1
FEI Numbers
114
Registration Numbers
114
Same Product Code
733
Applicant Total
11
Review Days
63

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Basic Information

Device Name
NUCLETRON PLANNING SYSTEM
K Number
K911612
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.5050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Nucletron-Oldelft Corp.
Date Received
April 11, 1991
Decision Date
June 13, 1991
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 Nucletron-Oldelft Corp.

K Number Device Name
K953946 MICROSELECTRON-HDR VERSION 2
K953831 N 800 HF
K925956 MICROSELECTRON - HDR FOR MOBILE ENVIRONMENT
K926407 MODEL COLE TAB-2 TABLE W/MODEL COLE SFD-2 SPOTFILM
K921991 PLATO RADIATION THERAPY PLANNING SYSTEM
K915622 PLATO BRACHYTHERAPHY TREATMENT PLANNING SYSTEM
K902533 PULSED SELECTRON
K864210 MICROSELECTRON-HDR (HIGH DOSE RATE)
K853912 MICROSELECTION INTERSTITIAL REMOTE AFTERLOAD SYS
K852842 SELECTRON HDR REMOTE AFTERLOADER
Search all 11 clearances from Nucletron-Oldelft Corp. →