FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇪 Germany

PHILIPS ANESTHESIA GAS MONITOR, MODEL M1026B

K Number: K040917 · Decision Apr 29, 2004
Classifications
1
FEI Numbers
55
Registration Numbers
55
Same Product Code
21
Applicant Total
48
Review Days
21

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Basic Information

Device Name
PHILIPS ANESTHESIA GAS MONITOR, MODEL M1026B
K Number
K040917
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
868.1500
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Philips Medizin Systeme Boeblingen GmbH
Date Received
April 8, 2004
Decision Date
April 29, 2004
Product Code
CBQ
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
CBQ Analyzer, Gas, Enflurane, Gaseous-Phase (Anesthetic Concentration)

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K230604 IntelliVue Patient Monitor MX100 (867033), IntelliVue Multi-Measurement Module X3 (867030)
K223574 IntelliVue Patient Monitor MX400 (866060), IntelliVue Patient Monitor MX450 (866062), IntelliVue Patient Monitor MX500 (866064), IntelliVue Patient Monitor MX550 (866066)
K210906 IntelliVue Patient Monitor MX750, IntelliVue Patient Monitor MX850, IntelliVue 4-Slot module rack FMX-4
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K192137 IntelliVue Patient Monitor MX500, IntelliVue Patient Monitor MX550
K182979 IntelliVue Patient Monitors MX100, MX400, MX430, MX450, MX500, MX550, IntelliVue Patient Monitors MX700, MX800, IntelliVue Patient Monitors MP5, MP5SC, Multi-Measurement Module X3
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