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FDA 510(k)

OXYCON PRO

K-Number: K992214 · 2000-02-22

Decision Date2000-02-22
Product CodeBZC
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

OXYCON PRO is the device name listed in this FDA 510(k) record. The listed applicant is Erich Jaeger B.V.. It received FDA 510(k) clearance on 2000-02-22 under 510(k) number K992214. 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 PRO?

OXYCON PRO is a medical device that received FDA 510(k) clearance on 2000-02-22. The listed applicant is Erich Jaeger B.V.. The 510(k) number is K992214.

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

OXYCON PRO received FDA 510(k) clearance on 2000-02-22, under 510(k) number K992214.

Who is the listed applicant for OXYCON PRO?

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

What is the FDA product code for OXYCON PRO?

The FDA product code for OXYCON PRO is BZC.

Related Clinical Trials

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.

Other records listing Erich Jaeger B.V. 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.

Related Devices (Code: BZC)

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.

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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