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

NIHON KOHDEN CENTRAL NURSE STATION, CNS-8310A/CNS-8350A

K Number: K935877 · Decision May 24, 1995
Classifications
1
FEI Numbers
121
Registration Numbers
121
Same Product Code
395
Applicant Total
166
Review Days
531

Basic Information

Device Name
NIHON KOHDEN CENTRAL NURSE STATION, CNS-8310A/CNS-8350A
K Number
K935877
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1025
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
NIHON KOHDEN AMERICA, INC.
Date Received
December 9, 1993
Decision Date
May 24, 1995
Product Code
DSI
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
DSI Detector And Alarm, Arrhythmia

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