FDA 510(k) Substantially Equivalent 🇺🇸 United States

NIHON KOHDEN ECG-9110K AND ECG-9130K CARDIOFAX Q AND ACCESSORIES

K Number: K984504 · Decision Apr 15, 1999
Classifications
0
FEI Numbers
11
Registration Numbers
11
Same Product Code
82
Applicant Total
166
Review Days
118

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Basic Information

Device Name
NIHON KOHDEN ECG-9110K AND ECG-9130K CARDIOFAX Q AND ACCESSORIES
K Number
K984504
Clearance Type
Traditional
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Nihon Kohden America, Inc.
Date Received
December 18, 1998
Decision Date
April 15, 1999
Product Code
LOS
Advisory Committee
Unknown
Review Advisory Committee
CV
Third Party
N

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