FDA 510(k)

PHILIPS ANESTHESIA GAS MONITOR, MODEL M1026B

K-Number: K040917 · 2004-04-29

ApplicantPhilips Medizin Systeme Boeblingen GmbH

Decision Date2004-04-29

Product CodeCBQ

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

PHILIPS ANESTHESIA GAS MONITOR, MODEL M1026B is the device name listed in this FDA 510(k) record. The listed applicant is Philips Medizin Systeme Boeblingen GmbH. It received FDA 510(k) clearance on 2004-04-29 under 510(k) number K040917. The device is classified under product code CBQ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHILIPS ANESTHESIA GAS MONITOR, MODEL M1026B?

PHILIPS ANESTHESIA GAS MONITOR, MODEL M1026B is a medical device that received FDA 510(k) clearance on 2004-04-29. The listed applicant is Philips Medizin Systeme Boeblingen GmbH. The 510(k) number is K040917.

When did PHILIPS ANESTHESIA GAS MONITOR, MODEL M1026B receive FDA 510(k) clearance?

PHILIPS ANESTHESIA GAS MONITOR, MODEL M1026B received FDA 510(k) clearance on 2004-04-29, under 510(k) number K040917.

Who is the listed applicant for PHILIPS ANESTHESIA GAS MONITOR, MODEL M1026B?

The FDA 510(k) record lists Philips Medizin Systeme Boeblingen GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PHILIPS ANESTHESIA GAS MONITOR, MODEL M1026B?

The FDA product code for PHILIPS ANESTHESIA GAS MONITOR, MODEL M1026B is CBQ.

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Related Devices (Code: CBQ)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.