FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

N 800 HF

K Number: K953831 · Decision Sep 8, 1995
Classifications
1
FEI Numbers
42
Registration Numbers
42
Same Product Code
162
Applicant Total
11
Review Days
24

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Basic Information

Device Name
N 800 HF
K Number
K953831
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
892.1700
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Nucletron-Oldelft Corp.
Date Received
August 15, 1995
Decision Date
September 8, 1995
Product Code
IZO
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
IZO Generator, High-Voltage, X-Ray, Diagnostic

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Other Clearances by Nucletron-Oldelft Corp.

K Number Device Name
K953946 MICROSELECTRON-HDR VERSION 2
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
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. →