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FDA 510(k)

OMNI 2 OXYGEN SYSTEM

K-Number: K083163 · 2009-10-20

Decision Date2009-10-20
Product CodeCAW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

OMNI 2 OXYGEN SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Sequal Technologies, Inc.. It received FDA 510(k) clearance on 2009-10-20 under 510(k) number K083163. The device is classified under product code CAW. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OMNI 2 OXYGEN SYSTEM?

OMNI 2 OXYGEN SYSTEM is a medical device that received FDA 510(k) clearance on 2009-10-20. The listed applicant is Sequal Technologies, Inc.. The 510(k) number is K083163.

When did OMNI 2 OXYGEN SYSTEM receive FDA 510(k) clearance?

OMNI 2 OXYGEN SYSTEM received FDA 510(k) clearance on 2009-10-20, under 510(k) number K083163.

Who is the listed applicant for OMNI 2 OXYGEN SYSTEM?

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

What is the FDA product code for OMNI 2 OXYGEN SYSTEM?

The FDA product code for OMNI 2 OXYGEN SYSTEM is CAW.

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 Sequal Technologies, Inc. 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: CAW)

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

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