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

DATEX-OHMEDA S/5 ENTROPY MODULE, M-ENTROPY AND ACCESSORIES

K Number: K023459 · Decision Jan 13, 2003
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
37
Applicant Total
40
Review Days
90

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Basic Information

Device Name
DATEX-OHMEDA S/5 ENTROPY MODULE, M-ENTROPY AND ACCESSORIES
K Number
K023459
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1400
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Datex-Ohmeda
Date Received
October 15, 2002
Decision Date
January 13, 2003
Product Code
OLW
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
OLW Index-Generating Electroencephalograph Software

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K043572 COMPATIBILITY ECG TRUNK CABLES
K043551 DATEX-OHMEDA S/5 PSM MODULE, (CONSISTING OF E-PSM AND E-PSMP MODULES) AND ACCESSORIES
K043276 DATEX-OHMEDA S/5TM FM WITH L-FICU04 AND L-FICU04A SOFTWARE AND N-FCREC MODULE
K042771 GE DATEX-OHMEDA S/5 NETWORK AND ICENTRAL '03, SALES REVISION 3.3
K041772 DATEX-OHMEDA PRESTN.01 MODULE (MODEL FAMILY M-PRESTN.01) AND ACCESSORIES
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