PORTABLE THERAPEUTIC LIQUID OXYGEN UNIT
K-Number: K880183 · 1988-04-14
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Device Summary
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.
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