ClearanceBrief
Company ยท US

Radkor, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1988 to 1989. Name variants (Inc, Corp, punctuation) are merged.

10510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
IYBTube Mount, X-Ray, Diagnostic3
IZOGenerator, High-Voltage, X-Ray, Diagnostic3
KXJTable, Radiologic2
IXQTable, Radiographic, Stationary Top1
IXYHolder, Radiographic Cassette, Wall-Mounted1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Nov 13, 1989K895969RADKOR DXG-650R
Radkor, Inc.
IZO
Apr 26, 1989K892196RADKOR TS10-B
Radkor, Inc.
IXQ
Apr 3, 1989K891395RADKOR BS-10 AND BS-10T
Radkor, Inc.
IXY
Oct 19, 1988K883885RADKOR, RF-159
Radkor, Inc.
KXJ
Oct 19, 1988K883864RADKOR SFR-70
Radkor, Inc.
IYB
Sep 8, 1988K881701RADKOR SFC-21
Radkor, Inc.
IYB
Sep 2, 1988K883081RADKOR, XG-515
Radkor, Inc.
IZO
Sep 2, 1988K881700RADKOR KOB-84
Radkor, Inc.
KXJ
Sep 2, 1988K881696RADKOR XG-325
Radkor, Inc.
IZO
Jul 8, 1988K882563RADKOR, CST-18
Radkor, Inc.
IYB

Latest recalls

DateFirm and productCodeLinked 510(k)
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