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

GE DATEX-OHMEDA AVANCE CS2

K Number: K131945 · Decision Aug 8, 2013
Classifications
1
FEI Numbers
33
Registration Numbers
33
Same Product Code
187
Applicant Total
40
Review Days
42

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Basic Information

Device Name
GE DATEX-OHMEDA AVANCE CS2
K Number
K131945
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
868.5160
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Datex-Ohmeda
Date Received
June 27, 2013
Decision Date
August 8, 2013
Product Code
BSZ
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

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

Product Code Device Name
BSZ Gas-Machine, Anesthesia

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K042891 DATEX-OHMEDA OXY-AFR SENSOR
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
K041790 DATEX-OHMEDA S/5 COMPACT ANESTHESIA MONITOR WITH L-CANE03 AND LCANE03A SOFTWARE
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