FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇭 Switzerland

ARGUS, MODEL LCM

K Number: K053207 · Decision May 19, 2006
Classifications
1
FEI Numbers
121
Registration Numbers
121
Same Product Code
411
Applicant Total
15
Review Days
184

Basic Information

Device Name
ARGUS, MODEL LCM
K Number
K053207
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1025
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
SCHILLER AG
Date Received
November 16, 2005
Decision Date
May 19, 2006
Product Code
MHX
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
MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)

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