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

FUTURUS 2001 X-RAY GENERATOR

K Number: K902637 · Decision Aug 3, 1990
Classifications
1
FEI Numbers
42
Registration Numbers
42
Same Product Code
162
Applicant Total
13
Review Days
50

Basic Information

Device Name
FUTURUS 2001 X-RAY GENERATOR
K Number
K902637
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
892.1700
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Acoma Medical Imaging, Inc.
Date Received
June 14, 1990
Decision Date
August 3, 1990
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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K944952 ANGIOGRAPHIC SYSTEM
K941017 F/C/W TUBESTAND
K941004 CTS SYSTEM
K925598 BUCKYMATIC AUTOMATIC CHEST FILM CHANGER
K921116 PX-100 PORTABLE X-RAY GENERATOR
K921425 SCD-105 AND SCD-125 CAPACITOR DISCHARGE MOBILE X-R
K900562 TRANS X 100 CHEST FILM CHANGER
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