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

PLURIX B; RADIOGRAPHIC TABLE

K Number: K781067 · Decision Jul 17, 1978
Classifications
1
FEI Numbers
22
Registration Numbers
22
Same Product Code
26
Applicant Total
18
Review Days
21

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Basic Information

Device Name
PLURIX B; RADIOGRAPHIC TABLE
K Number
K781067
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1980
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Tecnomed, Inc.
Date Received
June 26, 1978
Decision Date
July 17, 1978
Product Code
IXQ
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
IXQ Table, Radiographic, Stationary Top

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Other Clearances by Tecnomed, Inc.

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. →