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

AMBU NEUROLINE SINGLE PATIENT EEG/EP CUP ELECTRODE

K Number: K032278 · Decision Mar 5, 2004
Classifications
1
FEI Numbers
243
Registration Numbers
243
Same Product Code
436
Applicant Total
33
Review Days
225

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Basic Information

Device Name
AMBU NEUROLINE SINGLE PATIENT EEG/EP CUP ELECTRODE
K Number
K032278
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1320
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Ambu, Inc.
Date Received
July 24, 2003
Decision Date
March 5, 2004
Product Code
GXY
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
GXY Electrode, Cutaneous

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K041734 AMBU DISPOSABLE ECG ELECTRODE
K040991 AMBU DISPOSABLE PRESSURE MANOMETER
K041026 AMBU BLUE SENSOR, MRX, ECG ELECTRODE PRODUCT #:MRX-00-S
K032421 AMBU PEDIATRIC MULTI-FUNCTION DEFIBRILLATION ELECTRODE
K010583 AMBU GEL, HYDROGEL BURN DRESSING
K993278 AMBU NEONATE SILICONE RESUSCITATOR
K992902 AMBU HAND POWER SUCTION PUMP
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