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

TECHNY REX 3000 MOBILE X-RAY UNIT

K Number: K803103 · Decision Jan 22, 1981
Classifications
1
FEI Numbers
77
Registration Numbers
77
Same Product Code
235
Applicant Total
18
Review Days
44

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Basic Information

Device Name
TECHNY REX 3000 MOBILE X-RAY UNIT
K Number
K803103
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1720
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Tecnomed, Inc.
Date Received
December 9, 1980
Decision Date
January 22, 1981
Product Code
IZL
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
IZL System, X-Ray, Mobile

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K Number Device Name
K892226 TEC 6340 90/15 RADIOGRAPHIC/FLUOROSCOPIC TABLE
K854203 TEC 2720 MAMEX DC MAG
K827124 RALCO COLLIMATOR, AUTOMATIC, RADIOGRAPHIC
K820306 RALCO COLLIMATOR, AUTOMATIC RADIOGRAPHIC
K820307 TECNOMED GENERATOR, RADIOGRAPH., 3 PHASE
K827126 TECHNOMED GENERATOR, RADIOGRAPHIC, 3 PHASE
K827125 RALCO COLLIMATORS, MANUAL, RADIOGRAPHIC
K820305 RALCO COLLIMATORS, MANUAL RADIOGRAPHIC
K811197 SUPERIX 120
K811195 ARGOSTAT
Search all 18 clearances from Tecnomed, Inc. →