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

RADIOGRAPHIC/FLUOROSCOPIC TABLE MODEL 9004

K Number: K911267 · Decision Apr 3, 1991
Classifications
1
FEI Numbers
23
Registration Numbers
23
Same Product Code
76
Applicant Total
35
Review Days
23

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Basic Information

Device Name
RADIOGRAPHIC/FLUOROSCOPIC TABLE MODEL 9004
K Number
K911267
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1980
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Tri W-G, Inc.
Date Received
March 11, 1991
Decision Date
April 3, 1991
Product Code
IXR
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
IXR Table, Radiographic, Tilting

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Other Clearances by Tri W-G, Inc.

K Number Device Name
K960196 TRI W-G, INC TABLE, TILT/EXAM/TREATMENT MODEL 777
K945163 ECHOCARDIOGRAPHY
K941720 MODEL 747 AND 747-30 EXAM/TREATMENT TABLE
K936303 TREATMENT TABLE MODIFICATION
K933119 HI-LO TREATMENT TABLES
K932746 MODEL T4501,T4502,T4503,T4504,T4504 TILT TABLE
K930802 MODELS 642 & 643 TILT EXAM/TREATMENT TABLE
K925594 MDL 29001 MEDI ELEC-MECH TILT EXAM/TREATMENT TABLE
K923325 MODEL 600 MEDICAL TREATMENT TABLE
K922980 745-M (MAGNUM)
Search all 35 clearances from Tri W-G, Inc. →