GENERATOR, OXYGEN, PORTABLE
K-Number: K780020 · 1978-01-26
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Device Summary
Frequently Asked Questions
What is the GENERATOR, OXYGEN, PORTABLE?
GENERATOR, OXYGEN, PORTABLE is a medical device that received FDA 510(k) clearance on 1978-01-26. The listed applicant is Jet Research Center, Inc.. The 510(k) number is K780020.
When did GENERATOR, OXYGEN, PORTABLE receive FDA 510(k) clearance?
GENERATOR, OXYGEN, PORTABLE received FDA 510(k) clearance on 1978-01-26, under 510(k) number K780020.
Who is the listed applicant for GENERATOR, OXYGEN, PORTABLE?
The FDA 510(k) record lists Jet Research Center, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GENERATOR, OXYGEN, PORTABLE?
The FDA product code for GENERATOR, OXYGEN, PORTABLE 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 Jet Research Center, 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
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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