Spectrum X-Ray Corp. - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Spectrum X-Ray Corp. has 9 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 9 cleared submissions from 1979 to 1993. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Spectrum X-Ray Corp. Filter by specialty or product code using the sidebar.
9 devices
Cleared
Oct 07, 1993
SPECTRUM DG-P7000 PEDIATRIC CRADLE
Radiology
101d
Cleared
Aug 23, 1993
SPECTRUM MARK I SPECIAL PROCEDURES TABLE
Radiology
146d
Cleared
May 14, 1987
PENTAMAX 1 MODEL B TABLE SYSTEM
Radiology
83d
Cleared
Feb 21, 1984
SPECTRUM X-RAY CORP
Radiology
69d
Cleared
Feb 21, 1984
DIGITAL CRADLE
Radiology
19d
Cleared
May 19, 1982
SIMPLAMATIC III
Radiology
22d
Cleared
Jan 29, 1982
SPECTRUM PEDIATRIC CARDLE TABLE
Radiology
38d
Cleared
Nov 05, 1979
SPECTRUM EMERGENCY & TRAUMA TABLE SYSTEM
Radiology
48d
Cleared
Oct 26, 1979
SPECTRUM AUTOMATIC CHEST UNIT MODEL C
Radiology
38d