Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

PORTABLE THERAPEUTIC LIQUID OXYGEN UNIT

K-Number: K880183 · 1988-04-14

Decision Date1988-04-14
Product CodeBYJ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PORTABLE THERAPEUTIC LIQUID OXYGEN UNIT is the device name listed in this FDA 510(k) record. The listed applicant is Essex Cryogenics of Missouri, Inc.. It received FDA 510(k) clearance on 1988-04-14 under 510(k) number K880183. 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 PORTABLE THERAPEUTIC LIQUID OXYGEN UNIT?

PORTABLE THERAPEUTIC LIQUID OXYGEN UNIT is a medical device that received FDA 510(k) clearance on 1988-04-14. The listed applicant is Essex Cryogenics of Missouri, Inc.. The 510(k) number is K880183.

When did PORTABLE THERAPEUTIC LIQUID OXYGEN UNIT receive FDA 510(k) clearance?

PORTABLE THERAPEUTIC LIQUID OXYGEN UNIT received FDA 510(k) clearance on 1988-04-14, under 510(k) number K880183.

Who is the listed applicant for PORTABLE THERAPEUTIC LIQUID OXYGEN UNIT?

The FDA 510(k) record lists Essex Cryogenics of Missouri, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PORTABLE THERAPEUTIC LIQUID OXYGEN UNIT?

The FDA product code for PORTABLE THERAPEUTIC LIQUID OXYGEN UNIT 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.

Other records listing Essex Cryogenics of Missouri, 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: 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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑