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

PLATO BRACHYTHERAPHY TREATMENT PLANNING SYSTEM

K Number: K915622 · Decision Sep 25, 1992
Classifications
1
FEI Numbers
46
Registration Numbers
46
Same Product Code
206
Applicant Total
11
Review Days
284

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Basic Information

Device Name
PLATO BRACHYTHERAPHY TREATMENT PLANNING SYSTEM
K Number
K915622
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.5700
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Nucletron-Oldelft Corp.
Date Received
December 16, 1991
Decision Date
September 25, 1992
Product Code
JAQ
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
JAQ System, Applicator, Radionuclide, Remote-Controlled

Similar 510(k) Clearances

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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
K911612 NUCLETRON 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. →