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

EXT-600 TABLE, RADIOGRAPHIC, ELEVATING

K Number: K896665 · Decision Jan 22, 1990
Classifications
1
FEI Numbers
26
Registration Numbers
26
Same Product Code
28
Applicant Total
10
Review Days
56

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Basic Information

Device Name
EXT-600 TABLE, RADIOGRAPHIC, ELEVATING
K Number
K896665
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1980
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Rms Div.
Date Received
November 27, 1989
Decision Date
January 22, 1990
Product Code
IZZ
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
IZZ Table, Radiographic, Non-Tilting, Powered

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Other Clearances by Rms Div.

K Number Device Name
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K944848 THE VIVACARE T.P.S. PROBE
K944557 DW250 #91
K941625 DW234 #29
K902403 ELITE R/F SPOT FILM DRIVE
K902146 SFD-035 SPOT FILM DEVICE
K896119 RMS 90/15 RADIOGRAPHIC/FLUOROSCOPIC TILTING TABLE
K896324 ELITE 1500 RADIOGRAPHIC TILTING TABLE