FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

RADIONICS MICROELECTRODE KIT

K Number: K991399 · Decision Sep 21, 1999
Classifications
1
FEI Numbers
85
Registration Numbers
85
Same Product Code
65
Applicant Total
56
Review Days
152

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
RADIONICS MICROELECTRODE KIT
K Number
K991399
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.4725
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Radionics, Inc.
Date Received
April 22, 1999
Decision Date
September 21, 1999
Product Code
GXI
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GXI Probe, Radiofrequency Lesion

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (GXI), ordered by most recent decision date.

View all

Other Clearances by Radionics, Inc.

K Number Device Name
K030697 RADIONICS SINGLE USE GROUND PAD (DGP-HP)
K001741 RADIONICS RF DISC CATHETER ELECTRODE SYSTEM
K002773 NEUROMAP WITH NEURO 100
K992226 XDS EXTERNAL CSF DRAINAGE AND MONITORING SYSTEM
K001950 OPTICAL TRACKING SYSTEM (OTS)
K001700 XPLAN 2.1
K001431 MODIFICATION TO OPTICAL TRACKING SYSTEM (OTS)
K000057 RADIONICS LUMBOPERITONEAL SHUNT
K993594 CONFORMAX MMLC VR1
K992721 COSMAN ROBERT WELLS FUNCTIONAL PROBE MICRODRIVE
Search all 56 clearances from Radionics, Inc. →