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FDA 510(k)

LIQUID OXYGEN SYSTEM

K-Number: K032143 · 2004-03-30

Decision Date2004-03-30
Product CodeBYJ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

LIQUID OXYGEN SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Micro Technology Services, Inc.. It received FDA 510(k) clearance on 2004-03-30 under 510(k) number K032143. The device is classified under product code BYJ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIQUID OXYGEN SYSTEM?

LIQUID OXYGEN SYSTEM is a medical device that received FDA 510(k) clearance on 2004-03-30. The listed applicant is Micro Technology Services, Inc.. The 510(k) number is K032143.

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

LIQUID OXYGEN SYSTEM received FDA 510(k) clearance on 2004-03-30, under 510(k) number K032143.

Who is the listed applicant for LIQUID OXYGEN SYSTEM?

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

What is the FDA product code for LIQUID OXYGEN SYSTEM?

The FDA product code for LIQUID OXYGEN SYSTEM is BYJ.

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.

Related Devices (Code: BYJ)

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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