Nucletron-Oldelft Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Nucletron-Oldelft Corp. - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
Nucletron-Oldelft Corp. has 11 FDA 510(k) cleared radiology devices. Based in Columbia, US.
Historical record: 11 cleared submissions from 1986 to 1996.
Browse the complete list of FDA 510(k) cleared radiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Nucletron-Oldelft Corp.
11 devices
Cleared
Aug 13, 1996
MICROSELECTRON-HDR VERSION 2
Radiology
358d
Cleared
Sep 08, 1995
N 800 HF
Radiology
24d
Cleared
Nov 19, 1993
MICROSELECTRON - HDR FOR MOBILE ENVIRONMENT
Radiology
360d
Cleared
Mar 31, 1993
MODEL COLE TAB-2 TABLE W/MODEL COLE SFD-2 SPOTFILM
Radiology
100d
Cleared
Nov 27, 1992
PLATO RADIATION THERAPY PLANNING SYSTEM
Radiology
213d
Cleared
Sep 25, 1992
PLATO BRACHYTHERAPHY TREATMENT PLANNING SYSTEM
Radiology
284d
Cleared
Jun 13, 1991
NUCLETRON PLANNING SYSTEM
Radiology
63d
Cleared
Oct 12, 1990
PULSED SELECTRON
Radiology
126d
Cleared
Nov 26, 1986
MICROSELECTRON-HDR (HIGH DOSE RATE)
Radiology
29d
Cleared
May 21, 1986
MICROSELECTION INTERSTITIAL REMOTE AFTERLOAD SYS
Radiology
243d
Cleared
Jan 10, 1986
SELECTRON HDR REMOTE AFTERLOADER
Radiology
189d