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FDA 510(k)

DRAGER OXYLOG 2000

K-Number: K984577 · 1999-01-22

ApplicantDrager, Inc.
Decision Date1999-01-22
Product CodeCBK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

DRAGER OXYLOG 2000 is the device name listed in this FDA 510(k) record. The listed applicant is Drager, Inc.. It received FDA 510(k) clearance on 1999-01-22 under 510(k) number K984577. The device is classified under product code CBK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DRAGER OXYLOG 2000?

DRAGER OXYLOG 2000 is a medical device that received FDA 510(k) clearance on 1999-01-22. The listed applicant is Drager, Inc.. The 510(k) number is K984577.

When did DRAGER OXYLOG 2000 receive FDA 510(k) clearance?

DRAGER OXYLOG 2000 received FDA 510(k) clearance on 1999-01-22, under 510(k) number K984577.

Who is the listed applicant for DRAGER OXYLOG 2000?

The FDA 510(k) record lists Drager, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DRAGER OXYLOG 2000?

The FDA product code for DRAGER OXYLOG 2000 is CBK.

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Related Devices (Code: CBK)

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Official Source

View on FDA Database →

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

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