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

MR CONDITIONAL PRESSON ELECTRODE

K Number: K130220 · Decision Jul 22, 2013
Classifications
1
FEI Numbers
64
Registration Numbers
64
Same Product Code
52
Applicant Total
18
Review Days
174

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Basic Information

Device Name
MR CONDITIONAL PRESSON ELECTRODE
K Number
K130220
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1350
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Rhythmlink International, LLC
Date Received
January 29, 2013
Decision Date
July 22, 2013
Product Code
GXZ
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
GXZ Electrode, Needle

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Other Clearances by Rhythmlink International, LLC

K Number Device Name
K203079 MR Conditional Sticky Pad Electrode
K200984 Guardian Needle Electrode
K191225 EEG Electrode Template
K190801 PressOn Electrode Headset
K172503 MR Conditional Cup Electrode, MR Conditional Webb Electrode
K132138 RHYTHMLINK DISPOSABLE CONCENTRIC STIMULATING PROBE
K130287 MR CONDITIONAL CUP ELECTRODE, MR CONDITIONAL WEBB ELECTRODE
K121347 PRESSON ELECTRODE
K120342 EMG RECORDING ELECTRODE ASSEMBLY
K112435 RHYTHMLINK MONOPOLAR STIMULATING INSTRUMENT
Search all 18 clearances from Rhythmlink International, LLC →