P.O.G.S. 3.3 PORTABLE OXYGEN GENERATOR SYSTEM
K-Number: K020362 · 2002-02-12
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Device Summary
Frequently Asked Questions
What is the P.O.G.S. 3.3 PORTABLE OXYGEN GENERATOR SYSTEM?
P.O.G.S. 3.3 PORTABLE OXYGEN GENERATOR SYSTEM is a medical device that received FDA 510(k) clearance on 2002-02-12. The listed applicant is On Site Gas Systems, Inc.. The 510(k) number is K020362.
When did P.O.G.S. 3.3 PORTABLE OXYGEN GENERATOR SYSTEM receive FDA 510(k) clearance?
P.O.G.S. 3.3 PORTABLE OXYGEN GENERATOR SYSTEM received FDA 510(k) clearance on 2002-02-12, under 510(k) number K020362.
Who is the listed applicant for P.O.G.S. 3.3 PORTABLE OXYGEN GENERATOR SYSTEM?
The FDA 510(k) record lists On Site Gas Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for P.O.G.S. 3.3 PORTABLE OXYGEN GENERATOR SYSTEM?
The FDA product code for P.O.G.S. 3.3 PORTABLE OXYGEN GENERATOR SYSTEM 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 On Site Gas Systems, 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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