Medical Device Manufacturer · US , Walker , MI

Radionics, Inc. - FDA 510(k) Cleared Devices

56 submissions · 56 cleared · Since 1982

Total

Cleared

Denied

Radionics, Inc. has 56 FDA 510(k) cleared medical devices. Based in Walker, US.

Historical record: 56 cleared submissions from 1982 to 2003. Primary specialty: Neurology.

Browse the FDA 510(k) cleared devices submitted by Radionics, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Radionics, Inc.

56 devices

1-12 of 56

Cleared Apr 04, 2003

RADIONICS SINGLE USE GROUND PAD (DGP-HP)

K030697 · GEI

General & Plastic Surgery · 29d

Cleared Oct 23, 2000

RADIONICS RF DISC CATHETER ELECTRODE SYSTEM

K001741 · HRX

Orthopedic · 137d

Cleared Oct 23, 2000

NEUROMAP WITH NEURO 100

K002773 · GWF

Neurology · 47d

Cleared Aug 04, 2000

XDS EXTERNAL CSF DRAINAGE AND MONITORING SYSTEM

K992226 · JXG

Neurology · 399d

Cleared Jul 26, 2000

OPTICAL TRACKING SYSTEM (OTS)

MODIFICATION TO OPTICAL TRACKING SYSTEM (OTS)

K001431 · HAW

Neurology · 9d

Cleared Mar 20, 2000

RADIONICS LUMBOPERITONEAL SHUNT

RADIONICS MICROELECTRODE KIT

K991399 · GXI

Neurology · 152d

Cleared Sep 10, 1999

COSMAN ROBERT WELLS FUNCTIONAL PROBE MICRODRIVE

K992721 · HAW

Neurology · 28d

Cleared Sep 08, 1999

RADIONICS XDC EXTERNAL VENTRICULAR CATHETER

K992379 · JXG

Neurology · 54d

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Radionics, Inc. - FDA 510(k) Cleared Devices

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