FDA 510(k) FDA class 3 Substantially Equivalent 🇺🇸 United States

AMBU PEDIATRIC MULTI-FUNCTION DEFIBRILLATION ELECTRODE

K Number: K032421 · Decision Feb 27, 2004
Classifications
1
FEI Numbers
64
Registration Numbers
64
Same Product Code
227
Applicant Total
33
Review Days
206

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Basic Information

Device Name
AMBU PEDIATRIC MULTI-FUNCTION DEFIBRILLATION ELECTRODE
K Number
K032421
Device Class
FDA class 3
Clearance Type
Traditional
Regulation Number
870.5310
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Ambu, Inc.
Date Received
August 5, 2003
Decision Date
February 27, 2004
Product Code
MKJ
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

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

Product Code Device Name
MKJ Automated External Defibrillators (Non-Wearable)

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K Number Device Name
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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
K032278 AMBU NEUROLINE SINGLE PATIENT EEG/EP CUP ELECTRODE
K010583 AMBU GEL, HYDROGEL BURN DRESSING
K993278 AMBU NEONATE SILICONE RESUSCITATOR
K992902 AMBU HAND POWER SUCTION PUMP
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