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

DATEX-OHMEDA S/5TM FM WITH L-FICU04 AND L-FICU04A SOFTWARE AND N-FCREC MODULE

K Number: K043276 · Decision Dec 23, 2004
Classifications
1
FEI Numbers
121
Registration Numbers
121
Same Product Code
411
Applicant Total
40
Review Days
27

Basic Information

Device Name
DATEX-OHMEDA S/5TM FM WITH L-FICU04 AND L-FICU04A SOFTWARE AND N-FCREC MODULE
K Number
K043276
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1025
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
DATEX-OHMEDA
Date Received
November 26, 2004
Decision Date
December 23, 2004
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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