Radionics, A Division of Tyco Healthcare Group LP is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Radionics, A Division of Tyco Healthcare Group LP - FDA 510(k) Cleare...
8
Total
8
Cleared
0
Denied
Radionics, A Division of Tyco Healthcare Group LP has 8 FDA 510(k) cleared medical devices. Based in Burlington, US.
Historical record: 8 cleared submissions from 2001 to 2005. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Radionics, A Division of Tyco Healthcare Group LP Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Radionics, A Division of Tyco Healthcare Group LP
8 devices
Cleared
Aug 22, 2005
RADIONICS CUSA EXCEL ULTRASONIC SURGICAL ASPIRATOR SYSTEM WITH BONE
General & Plastic Surgery
35d
Cleared
Aug 27, 2004
RADIONICS XKNIFE RT 3 WITH NON STEREOTACTIC MODULE
Radiology
32d
Cleared
Sep 15, 2003
RADIONICS NASHOLD BIOPSY NEEDLE - SINGLE USE
Neurology
75d
Cleared
Jan 16, 2003
RADIONICS VARILINK 2
Radiology
87d
Cleared
Sep 11, 2002
RADIONICS POLE NEEDLES
Neurology
90d
Cleared
Dec 03, 2001
XPLAN 2.2 WITH THE BODY SYSTEM
Radiology
27d
Cleared
Nov 19, 2001
RECORDING AND STIMULATING ELECTRODE
Neurology
87d
Cleared
Mar 12, 2001
MODIFICATION TO OPTICAL TRACKING SYSTEM (OTS)
Neurology
14d