LIQUID OXYGEN UNIT, PORTABLE 73BYJ
K-Number: K780098 · 1978-03-02
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Device Summary
Frequently Asked Questions
What is the LIQUID OXYGEN UNIT, PORTABLE 73BYJ?
LIQUID OXYGEN UNIT, PORTABLE 73BYJ is a medical device that received FDA 510(k) clearance on 1978-03-02. The listed applicant is Andonian Cryogenics, Inc.. The 510(k) number is K780098.
When did LIQUID OXYGEN UNIT, PORTABLE 73BYJ receive FDA 510(k) clearance?
LIQUID OXYGEN UNIT, PORTABLE 73BYJ received FDA 510(k) clearance on 1978-03-02, under 510(k) number K780098.
Who is the listed applicant for LIQUID OXYGEN UNIT, PORTABLE 73BYJ?
The FDA 510(k) record lists Andonian Cryogenics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LIQUID OXYGEN UNIT, PORTABLE 73BYJ?
The FDA product code for LIQUID OXYGEN UNIT, PORTABLE 73BYJ 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
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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