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FDA 510(k)

OXYLOG 1000, MODEL 2M86840

K-Number: K010793 · 2001-12-20

ApplicantDrager Medizintechnik GmbH
Decision Date2001-12-20
Product CodeCBK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

OXYLOG 1000, MODEL 2M86840 is the device name listed in this FDA 510(k) record. The listed applicant is Drager Medizintechnik GmbH. It received FDA 510(k) clearance on 2001-12-20 under 510(k) number K010793. 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 OXYLOG 1000, MODEL 2M86840?

OXYLOG 1000, MODEL 2M86840 is a medical device that received FDA 510(k) clearance on 2001-12-20. The listed applicant is Drager Medizintechnik GmbH. The 510(k) number is K010793.

When did OXYLOG 1000, MODEL 2M86840 receive FDA 510(k) clearance?

OXYLOG 1000, MODEL 2M86840 received FDA 510(k) clearance on 2001-12-20, under 510(k) number K010793.

Who is the listed applicant for OXYLOG 1000, MODEL 2M86840?

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

What is the FDA product code for OXYLOG 1000, MODEL 2M86840?

The FDA product code for OXYLOG 1000, MODEL 2M86840 is CBK.

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Other records listing Drager Medizintechnik GmbH as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: CBK)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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