Medical Device Manufacturer · US , Burlington , MA

Radionics, A Division of Tyco Healthcare Group LP - FDA 510(k) Cleare...

8 submissions · 8 cleared · Since 2001
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
1-8 of 8
Cleared Aug 22, 2005
RADIONICS CUSA EXCEL ULTRASONIC SURGICAL ASPIRATOR SYSTEM WITH BONE
K051947 · LFL
General & Plastic Surgery · 35d
Cleared Aug 27, 2004
RADIONICS XKNIFE RT 3 WITH NON STEREOTACTIC MODULE
K041997 · MUJ
Radiology · 32d
Cleared Sep 15, 2003
RADIONICS NASHOLD BIOPSY NEEDLE - SINGLE USE
K032054 · HAW
Neurology · 75d
Cleared Jan 16, 2003
RADIONICS VARILINK 2
K023519 · IYE
Radiology · 87d
Cleared Sep 11, 2002
RADIONICS POLE NEEDLES
K021942 · GXI
Neurology · 90d
Cleared Dec 03, 2001
XPLAN 2.2 WITH THE BODY SYSTEM
K013661 · MUJ
Radiology · 27d
Cleared Nov 19, 2001
RECORDING AND STIMULATING ELECTRODE
K012850 · GZL
Neurology · 87d
Cleared Mar 12, 2001
MODIFICATION TO OPTICAL TRACKING SYSTEM (OTS)
K010548 · HAW
Neurology · 14d
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All8 Neurology 4 Radiology 3 General & Plastic Surgery 1