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

NEUROLINE, SUBDERMAL NEEDLE ELECTRODES

K Number: K020907 · Decision Jun 14, 2002
Classifications
1
FEI Numbers
39
Registration Numbers
39
Same Product Code
42
Applicant Total
7
Review Days
86

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Basic Information

Device Name
NEUROLINE, SUBDERMAL NEEDLE ELECTRODES
K Number
K020907
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.1385
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Medicotest A/S
Date Received
March 20, 2002
Decision Date
June 14, 2002
Product Code
IKT
Advisory Committee
Physical Medicine
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
IKT Electrode, Needle, Diagnostic Electromyograph

Similar 510(k) Clearances

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

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Other Clearances by Medicotest A/S

K Number Device Name
K020382 BLUE SENSOR, DISPOSABLE ECG ELECTRODES FOR ANAESTHESIA
K002079 MULTI-FUNCTION DEFIBRILLATION ELECTRODE
K001869 DIAGNOSTIC ELECTROMYOGRAPHY NEEDLE ELECTRODE, DISPOSABLE HYPODERMIC NEEDLE
K983689 BLUE SENSOR SUPATAB,DISPOSABLE ECG ELECTRODES
K973529 NEUROLINE, DISPOSABLE CONCENTRIC NEEDLE ELECTRODES
K965194 MEDICOM, TENS ELECTRODES