ClearanceBrief
Company ยท US

Pausch Corp.

FDA 510(k) clearances and medical device recalls filed under this name, 1979 to 2008. Name variants (Inc, Corp, punctuation) are merged.

9510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
IZFSystem, X-Ray, Tomographic2
KPRSystem, X-Ray, Stationary2
IXRTable, Radiographic, Tilting1
IXYHolder, Radiographic Cassette, Wall-Mounted1
IYBTube Mount, X-Ray, Diagnostic1
KXJTable, Radiologic1
OWBInterventional Fluoroscopic X-Ray System1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Dec 5, 2008K081073HDR VISION, VISION HDR, HD R/F, UROMAT HD R/F
Pausch, LLC
OWB
Jun 17, 1998K973864COMBI ELEVATOR-2 & COMBI ELEVATOR-2 TOMO
Pausch Corp.
IZF
Apr 30, 1998K973834CS2000 & CS2000 TOMO
Pausch Corp.
IZF
Aug 30, 1990K903395UROMAT 2000
Pausch Corp.
IXR
Mar 30, 1987K870856COSMOS
Pausch Corp.
IYB
Apr 26, 1979K790742KS-78 VERTICAL WALL CASSETTE HOLDER
Pausch Corp.
IXY
Apr 26, 1979K790741COMPACT SYSTEM
Pausch Corp.
KPR
Apr 26, 1979K790740BS 66, UNIVERSAL BUCKY STAND
Pausch Corp.
KPR
Apr 23, 1979K790743COORDINATUS, HORIZONTAL RADIOGRAPHOC
Pausch Corp.
KXJ

Latest recalls

DateFirm and productCodeLinked 510(k)
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