FDA 510(k) FDA class 2 Substantially Equivalent 🇯🇵 Japan

DISPOSAL ECG ELECTRODES, MODEL EASYRODE

K Number: K092389 · Decision Oct 13, 2009
Classifications
1
FEI Numbers
191
Registration Numbers
191
Same Product Code
328
Applicant Total
13
Review Days
69

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Basic Information

Device Name
DISPOSAL ECG ELECTRODES, MODEL EASYRODE
K Number
K092389
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2360
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Suzuken Co., Ltd.
Date Received
August 5, 2009
Decision Date
October 13, 2009
Product Code
DRX
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
DRX Electrode, Electrocardiograph

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Other Clearances by Suzuken Co., Ltd.

K Number Device Name
K172068 Kenz Cardico1211
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K870443 KENZ-CARDICO 1201
K862544 KENZ-ECG-102 SINGLE CHANNEL ELECTROCARDIOGRAPH
K843731 KENZ 80Z MARK II
K822968 ELECTROCARDIOGRAPH INTERPRETER
K820854 KENZ-45M
K820991 KENZ-GELECT GEL PAD
K812263 KENZ-GELECT
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