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

MICROSELECTRON-HDR (HIGH DOSE RATE)

K Number: K864210 · Decision Nov 26, 1986
Classifications
1
FEI Numbers
46
Registration Numbers
46
Same Product Code
206
Applicant Total
11
Review Days
29

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Basic Information

Device Name
MICROSELECTRON-HDR (HIGH DOSE RATE)
K Number
K864210
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.5700
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Nucletron-Oldelft Corp.
Date Received
October 28, 1986
Decision Date
November 26, 1986
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

Other 510(k) clearances with the same product code (JAQ), ordered by most recent decision date.

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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
K911612 NUCLETRON PLANNING SYSTEM
K902533 PULSED SELECTRON
K853912 MICROSELECTION INTERSTITIAL REMOTE AFTERLOAD SYS
K852842 SELECTRON HDR REMOTE AFTERLOADER
Search all 11 clearances from Nucletron-Oldelft Corp. →