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FDA 510(k)

OXYCON MOBILE

K-Number: K023120 · 2003-11-12

ApplicantErich Jaeger GmbH
Decision Date2003-11-12
Product CodeBZC
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

OXYCON MOBILE is the device name listed in this FDA 510(k) record. The listed applicant is Erich Jaeger GmbH. It received FDA 510(k) clearance on 2003-11-12 under 510(k) number K023120. The device is classified under product code BZC. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OXYCON MOBILE?

OXYCON MOBILE is a medical device that received FDA 510(k) clearance on 2003-11-12. The listed applicant is Erich Jaeger GmbH. The 510(k) number is K023120.

When did OXYCON MOBILE receive FDA 510(k) clearance?

OXYCON MOBILE received FDA 510(k) clearance on 2003-11-12, under 510(k) number K023120.

Who is the listed applicant for OXYCON MOBILE?

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

What is the FDA product code for OXYCON MOBILE?

The FDA product code for OXYCON MOBILE is BZC.

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Other records listing Erich Jaeger GmbH as applicant

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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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