ClearanceBrief
Company ยท US

Spectrum X-Ray Corp.

FDA 510(k) clearances and medical device recalls filed under this name, 1979 to 1993. 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
IXRTable, Radiographic, Tilting3
KXHCradle, Patient, Radiologic3
IZZTable, Radiographic, Non-Tilting, Powered1
KPXChanger, Radiographic Film/Cassette1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Oct 7, 1993K933134SPECTRUM DG-P7000 PEDIATRIC CRADLE
Spectrum X-Ray Corp.
KXH
Aug 23, 1993K931563SPECTRUM MARK I SPECIAL PROCEDURES TABLE
Spectrum X-Ray Corp.
IXR
May 14, 1987K870707PENTAMAX 1 MODEL B TABLE SYSTEM
Spectrum X-Ray Corp.
IXR
Feb 21, 1984K840463DIGITAL CRADLE
Spectrum X-Ray Corp.
KXH
Feb 21, 1984K834494SPECTRUM X-RAY CORP
Spectrum X-Ray Corp.
IZZ
May 19, 1982K827450SIMPLAMATIC III
Spectrum X-Ray Corp.
Jan 29, 1982K813561SPECTRUM PEDIATRIC CARDLE TABLE
Spectrum X-Ray Corp.
KXH
Nov 5, 1979K791812SPECTRUM EMERGENCY & TRAUMA TABLE SYSTEM
Spectrum X-Ray Corp.
IXR
Oct 26, 1979K791811SPECTRUM AUTOMATIC CHEST UNIT MODEL C
Spectrum X-Ray Corp.
KPX

Latest recalls

DateFirm and productCodeLinked 510(k)
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