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

GX-2000 STATIONARY X-RAY GENERATOR

K Number: K890083 · Decision Mar 31, 1989
Classifications
1
FEI Numbers
42
Registration Numbers
42
Same Product Code
162
Applicant Total
14
Review Days
80

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Basic Information

Device Name
GX-2000 STATIONARY X-RAY GENERATOR
K Number
K890083
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
892.1700
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Gendex Corp.
Date Received
January 10, 1989
Decision Date
March 31, 1989
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 Gendex Corp.

K Number Device Name
K952598 GX-PAN PANORAMIC DENTAL X-RAY SYSTEM
K945682 PROCESSOR, RADIOGRAPHIC-FILM, AUTOMATIC, DENTAL
K935046 GX-770 X-RAY CONTROL, MODEL 46-404600G4
K925094 VISUALIX RADIOGRAPHIC IMAGE DETECTING AND PROCESS
K931001 ORALIX DC
K932675 GXP DENTAL X-RAY PROCESSOR
K922165 ATC725, ATC525, AND AP300
K920189 GX-C CEPHALOMETER
K894188 GX-ELEVATOR
K873982 GX-MOBILE X-RAY UNIT
Search all 14 clearances from Gendex Corp. →